4,635 results on '"coloboma"'
Search Results
2. Potential Environmental Causes of Uveal Coloboma
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- 2024
3. A More Engaging Visual Field Test to Increase Use and Reliability in Pediatrics
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- 2024
4. Microphthalmia, Anophthalmia, and Coloboma Genetic Epidemiology in Children (MAGIC)
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National Eye Institute (NEI), National Institutes of Health (NIH), and Philip J Lupo, Principal Investigator, Professor of Pediatrics; Director, Epidemiology and Population Sciences Program
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- 2024
5. Ophthalmologic manifestations of organoid nevus syndrome: A series of 13 cases.
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Singh, Pallavi, Bajaj, Mandeep S., Agrawal, Sahil, Kaginalkar, Ananya, and Das, Deepsekhar
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OCULAR manifestations of general diseases ,NEVUS ,EYE care ,ECTOPIC tissue ,TERTIARY care - Abstract
The organoid nevus syndrome is a rare neurocutaneous syndrome typified by cutaneous sebaceous nevus, seizures and epibulbar choristomas. The condition is associated with multiple ocular abnormalities. Herein, the authors aim to study and report the ophthalmic features of cases diagnosed with organoid nevus syndrome. The authors retrospectively evaluated the records of patients with the organoid nevus syndrome who had presented to a tertiary care eye hospital in northern India. The ocular features were studied and entered in MS excel and the data were evaluated. Data of 13 patients with the organoid nevus syndrome were found. All 13 patients had cutaneous features in the form of Sebaceous nevus of Jadasson, 8 patients had alopecia of the scalp area, 2 had history seizures and 10 had arachnoid cysts on neuroimaging of the head. All 13 patients had a complex choristoma involving the ocular surface. We conclude that the most common ophthalmologic features associated with organoid nevus are complex choristoma of the bulbar surface, scleral coat calcification and upper eyelid coloboma. [ABSTRACT FROM AUTHOR]
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- 2024
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6. One-step repair of a large congenital upper eyelid coloboma using a bilamellar graft in an infant: a case report and literature review.
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Evereklioglu, Cem, Sener, Hidayet, Polat, Osman Ahmet, Gulmez Sevim, Duygu, Arda, Hatice, and Horozoglu, Fatih
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LITERATURE reviews , *EYELIDS , *MEDICAL care costs , *INFANTS , *REOPERATION - Abstract
Large congenital lid colobomas are traditionally repaired using 1- or 2-step vascularized flap-graft combinations. However, visual axis occlusion for weeks is a severe problem in small children and recent reports suggest that the flap pedicle does not contribute to blood perfusion. A "one-step" substitute for large lid defects has recently been reported in animals and humans, demonstrating the viability of a bilamellar autograft alone. We present an alternative "one-step" reconstructive approach in a 6-month-old infant who had a centrally-located large upper eyelid defect resulting from a congenital coloboma. The free full-thickness bilamellar autograft was harvested from the contralateral upper eyelid. The follow-up time was 48 months. Cosmetic and functional results were good, the bilamellar graft survived, and there was no graft ischemia, necrosis, or rejection. The boy developed madarosis, lid notching, and mild contour irregularity but needed no reoperation since the parent was satisfied with the surgical result. A free bilamellar eyelid autograft seems to be an outstanding alternative to both "conventional 2-step" and "modern 1-step" options for the reconstruction of large colobomatous eyelid openings, especially in young infants who cannot tolerate visual axis blockage. It is an easy, practical, fast, and effective technique that also saves cost in health care. [ABSTRACT FROM AUTHOR]
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- 2024
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7. Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysis.
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Kanwar, Kunal, Bashey, Saffiya, Bohnsack, Brenda L., Drackley, Andy, Ing, Alexander, Rahmani, Safa, Ranaivo, Hantamalala Ralay, McMullen, Patrick, Skol, Andrew, Yap, Kailee, Allegretti, Valerie, and Rossen, Jennifer L.
- Abstract
CHARGE syndrome is a rare multi‐system condition associated with CHD7 variants. However, ocular manifestations and particularly ophthalmic genotype–phenotype associations, are not well‐studied. This study evaluated ocular manifestations and genotype–phenotype associations in pediatric patients with CHARGE syndrome. A retrospective chart review included pediatric patients under 20 years‐old with clinical diagnosis of CHARGE syndrome and documented ophthalmic examination. Demographics, genetic testing, and ocular findings were collected. Comprehensive literature review enhanced the genotype–phenotype analysis. Forty‐two patients (20 male) underwent eye examination at an average age of 9.45 ± 6.52 years‐old. Thirty‐nine (93%) had ophthalmic manifestations in at least one eye. Optic nerve/chorioretinal colobomas were most common (38 patients), followed by microphthalmia (13), cataract (6), and iris colobomas (4). Extraocular findings included strabismus (32 patients), nasolacrimal duct obstructions (11, 5 with punctal agenesis), and cranial nerve VII palsy (10). Genotype–phenotype analyses (27 patients) showed variability in ocular phenotypes without association to location or variant types. Splicing (10 patients) and frameshift (10) variants were most prevalent. Patients with CHARGE syndrome may present with a myriad of ophthalmic manifestations. There is limited data regarding genotype–phenotype correlations and additional studies are needed. [ABSTRACT FROM AUTHOR]
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- 2024
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8. CHARGE Syndrome in a Newborn with Rearrangement of Chromosomes 15 and Y. Case Report
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Lina Marcela Barrera-Arenas, Camila Andrea Vargas-Londoño, Valentina Muñetón-Echeverry, Sebastián Álvarez-Giraldo, Edison Alexander Uribe-Graciano, and Laura Vanesa Díaz-Ruiz
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coloboma ,charge syndrome ,congenital abnormalities ,mutation ,Medicine ,Medicine (General) ,R5-920 - Abstract
Preterm neonate of 35+4 weeks, delivered by cesarean section due to non-reassuring fetal status. Prenatal ultrasound history of intrauterine growth restriction, cardiac malformations, and suspected central nervous system abnormalities. At birth, the neonate presented with a dysmorphic syndrome, choanal atresia, low ear implantation with bilateral malformation of the auricular pavilions and micropenis. The karyotype reported variants in chromosomes 15 and Y. A medical genetics specialist clinically diagnosed CHARGE syndrome. The patient received multidisciplinary management, requiring invasive mechanical ventilation, tracheostomy, thoracostomy and gastrostomy. He was discharged but readmitted due to aspiration pneumonia and died before a molecular diagnosis of the presence of a pathogenic variant for CHD7 could be made. This report constitutes a case of clinical diagnosis of CHARGE syndrome that presented structural alterations in chromosomes 15 and Y, which have not been described or associated in the literature as responsible for the etiology of this syndrome.
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- 2024
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9. Corpus callosal agenesis with gray matter heterotopia and bilateral eye coloboma in an infant: A case report
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Saubhagya Dhakal, Saroj Kumar Jha, Alisha Adhikari, Pinky Jha, and Srijana Katwal
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Corpus callosal agenesis ,Coloboma ,Case report ,Heterotopia ,Magnetic resonance imaging ,Medical physics. Medical radiology. Nuclear medicine ,R895-920 - Abstract
Corpus callosal agenesis (CCA) is a rare congenital disorder characterized by the partial or complete absence of the corpus callosum, a structure crucial for interhemispheric communication. CCA can occur in isolation or be associated with other anomalies such as heterotopia, holoprosencephaly, cerebellar hypoplasia, coloboma, and hydrocephalus. The prevalence of CCA ranges from 0.020% to 0.025%, though some reports suggest higher rates. This case report describes a 1-year-old male with developmental delays and no significant antenatal or family history. MRI revealed a complete absence of the corpus callosum, asymmetrically dilated lateral ventricles, subependymal gray matter nodules suggestive of gray matter heterotopia, and bilateral posterior globe defects with vitreous herniation, indicating severe ocular anomalies. The child received supportive care including physical therapy and special education services, with regular follow-ups for developmental and ophthalmologic evaluation. This case report details the rare occurrence of CCA, accompanied by gray matter heterotopia and bilateral posterior eye coloboma in a pediatric patient. The combination of these congenital anomalies presents unique diagnostic and management challenges requiring multidisciplinary care. We discuss the clinical presentation, radiological findings, and implications for supportive care and improving the prognosis.
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- 2024
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10. Congenital right optic nerve colobomatous cyst associated with microphthalmos
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Khadija Laasri, Yahya El harras, Zineb Izi, Zakia El yousfi, Jamal El fenni, and Issam En nafaa
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Optical nerve ,Coloboma ,Orbit ,MRI ,Medical physics. Medical radiology. Nuclear medicine ,R895-920 - Abstract
Optic nerve coloboma is a congenital defect caused by the incomplete closure of the embryonic fissure. This closure begins around the fifth week of gestation, when the embryo measures approximately 7 to 14 mm. Colobomas may appear as isolated defects or alongside other ocular and systemic abnormalities. They typically occur in the inferonasal quadrant, where the optic vesicle undergoes closure. This closure process starts centrally within the eye and progresses both anteriorly and posteriorly. The distinct nature of these closures can result in an optic nerve coloboma without an associated iris coloboma.The formation of a coloboma can be attributed to external factors affecting the fetus during pregnancy or to a genetic mutation, such as an autosomal dominant mutation in the Pax gene, which is linked to bilateral colobomas. Small colobomas generally require only clinical and radiological observation, whereas larger colobomas may need surgical intervention to remove the cyst and prevent complications related to orbital content development, thereby improving cosmetic outcomes
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- 2024
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11. Retinitis pigmentosa with iris coloboma due to miR‐204 gene variant in a Chinese family.
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Lei, Zhang, He‐Lin, Zhu, Hai‐Yan, Wang, Wei, Jia, Ru, Wang, Zhi‐Li, Cui, and Qian‐Feng, Wang
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RETINITIS pigmentosa , *GENETIC variation , *IRIS recognition , *VISION , *OPTICAL coherence tomography , *NON-coding RNA , *MISSENSE mutation - Abstract
Purpose: To characterize the phenotype and genotype of a Chinese family with autosomal‐dominant retinitis pigmentosa (RP) accompanied by iris coloboma. Methods: The proband, a 34‐year‐old male, was examined with his family by using fundus photography, optical coherence tomography (OCT), autofluorescence, and full‐field electroretinography (ffERG). Genetic analyses were conducted through whole‐exome sequencing (WES) to screen for variations. Results: Three members of this Chinese family were shown to be bilateral iris coloboma. The male proband and his mother exhibited typical RP feature. The proband's late grandfather had been documented manifestation of iris coloboma. The mode of inheritance was confirmed to be autosomal dominance. Through linkage analysis and WES, a heterozygous variation in the miR‐204 gene (n.37C>T), a noncoding RNA gene, was identified in these three members. Conclusions: In this third independent and the first Asian family, the existence of a miR‐204 variant associated with RP accompanied by iris coloboma was confirmed. Our findings reinforce the significance of miR‐204 as an important factor influencing visual function in the retina. When phenotypes like RP accompanied by iris coloboma in an autosomal‐dominant pattern, including in Chinese patients, miR‐204 aberrations should be considered. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
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12. Ocular manifestations of renal ciliopathies.
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Salehi, Omar, Mack, Heather, Colville, Deb, Lewis, Debbie, and Savige, Judy
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RISK assessment , *NEPHRITIS , *BIOLOGICAL models , *CILIOPATHY , *RESEARCH funding , *EYE abnormalities , *RETINAL diseases , *TUBEROUS sclerosis , *OCULAR manifestations of general diseases , *CYSTIC kidney disease , *POLYCYSTIC kidney disease , *GENETIC disorders , *COLOBOMA , *PHENOTYPES - Abstract
Renal ciliopathies are a common cause of kidney failure in children and adults, and this study reviewed their ocular associations. Genes affected in renal ciliopathies were identified from the Genomics England Panels. Ocular associations were identified from Medline and OMIM, and the genes additionally examined for expression in the human retina (https://www.proteinatlas.org/humanproteome/tissue) and for an ocular phenotype in mouse models (http://www.informatics.jax.org/). Eighty-two of the 86 pediatric-onset renal ciliopathies (95%) have an ocular phenotype, including inherited retinal degeneration, oculomotor disorders, and coloboma. Diseases associated with pathogenic variants in ANK6, MAPKBP1, NEK8, and TCTN1 have no reported ocular manifestations, as well as low retinal expression and no ocular features in mouse models. Ocular abnormalities are not associated with the most common adult-onset "cystic" kidney diseases, namely, autosomal dominant (AD) polycystic kidney disease and the AD tubulointerstitial kidney diseases (ADTKD). However, other kidney syndromes with cysts have ocular features including papillorenal syndrome (optic disc dysplasia), Hereditary Angiopathy Nephropathy, Aneurysms and muscle Cramps (HANAC) (tortuous retinal vessels), tuberous sclerosis (retinal hamartomas), von Hippel-Lindau syndrome (retinal hemangiomas), and Alport syndrome (lenticonus, fleck retinopathy). Ocular abnormalities are associated with many pediatric-onset renal ciliopathies but are uncommon in adult-onset cystic kidney disease. However the demonstration of ocular manifestations may be helpful diagnostically and the features may require monitoring or treatment. [ABSTRACT FROM AUTHOR]
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- 2024
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13. RECURRENT OPTIC DISC PIT MACULOPATHY DUE TO VALSALVA'S MANEUVER.
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Reis Cyrino, Francyne Veiga, Guzzi Marques, Joao Pedro, and Jorge, Rodrigo
- Abstract
Purpose: We report a patient with recurrent optic disc pit (ODP) maculopathy after Valsalva's maneuver and discuss its pathophysiology. We also hypothesize the role of Valsalva's maneuver in its genesis. Method: Case report of one patient, male, 12 years old. Results: Serous retinal detachment may occur in association with the ODP, a developmental anomaly of the optic nerve head. Histopathologically, it consists of a dysplastic retina herniation into a pocket extending posteriorly through a defect in the lamina cribrosa into the subarachnoid space. These three different compartments--intraocular space, optic nerve head, and subarachnoid space--and the dynamic interactions among them should be understood as the key factors for the occurrence of ODP-related serous retinal detachment. Conclusion: Based on the possibility that serous retinal detachment secondary to the ODP could be related to the Valsalva's maneuver, we strongly recommend that patients with ODP be advised to avoid intense physical or work activities that may increase abdominal, thoracic, and cerebral pressure and to refrain from playing wind instruments to avoid pretreatment, per treatment, and post-treatment intercurrences. [ABSTRACT FROM AUTHOR]
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- 2024
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14. Pervasive cortical and white matter anomalies in a mouse model for CHARGE syndrome
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Donovan, Alex PA, Rosko, Lauren, Ellegood, Jacob, Redhead, Yushi, Green, Jeremy BA, Lerch, Jason P, Huang, Jeffrey K, and Basson, M Albert
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Zoology ,Biological Sciences ,Clinical Research ,Rare Diseases ,Neurosciences ,Brain Disorders ,Biomedical Imaging ,Intellectual and Developmental Disabilities (IDD) ,Genetics ,Pediatric ,Congenital Structural Anomalies ,2.1 Biological and endogenous factors ,Aetiology ,Neurological ,Mice ,Animals ,CHARGE Syndrome ,White Matter ,Diffusion Tensor Imaging ,Autism Spectrum Disorder ,Coloboma ,Biomedical Engineering ,Medical Physiology ,Anatomy & Morphology - Abstract
CHARGE (Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth, Genital anomalies and Ear abnormalities) syndrome is a disorder caused by mutations in the gene encoding CHD7, an ATP dependent chromatin remodelling factor, and is characterised by a diverse array of congenital anomalies. These include a range of neuroanatomical comorbidities which likely underlie the varied neurodevelopmental disorders associated with CHARGE syndrome, which include intellectual disability, motor coordination deficits, executive dysfunction, and autism spectrum disorder. Cranial imaging studies are challenging in CHARGE syndrome patients, but high-throughput magnetic resonance imaging (MRI) techniques in mouse models allow for the unbiased identification of neuroanatomical defects. Here, we present a comprehensive neuroanatomical survey of a Chd7 haploinsufficient mouse model of CHARGE syndrome. Our study uncovered widespread brain hypoplasia and reductions in white matter volume across the brain. The severity of hypoplasia appeared more pronounced in posterior areas of the neocortex compared to anterior regions. We also perform the first assessment of white matter tract integrity in this model through diffusion tensor imaging (DTI) to assess the potential functional consequences of widespread reductions in myelin, which suggested the presence of white matter integrity defects. To determine if white matter alterations correspond to cellular changes, we quantified oligodendrocyte lineage cells in the postnatal corpus callosum, uncovering reduced numbers of mature oligodendrocytes. Together, these results present a range of promising avenues of focus for future cranial imaging studies in CHARGE syndrome patients.
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- 2023
15. Renal coloboma syndrome/dominant optic atrophy with severe retinal atrophy and de novo digenic mutations in PAX2 and OPA1.
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Shimabukuro, Wataru, Chinen, Yasutsugu, Imanaga, Naoya, Yanagi, Kumiko, Kaname, Tadashi, and Nakanishi, Koichi
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RETINAL disease diagnosis , *KIDNEY disease diagnosis , *OPTIC nerve diseases , *SEVERITY of illness index , *MAGNETIC resonance imaging , *PHOTOGRAPHY , *ELECTRORETINOGRAPHY , *GENETIC disorders , *URINALYSIS , *COLOBOMA , *GENETIC mutation , *BLINDNESS , *GENETIC techniques , *GLOMERULAR filtration rate , *KIDNEYS - Abstract
Renal coloboma syndrome (RCS) and dominant optic atrophy are mainly caused by heterozygous mutations in PAX2 and OPA1, respectively. We describe a patient with digenic mutations in PAX2 and OPA1. A female infant was born without perinatal abnormalities. Magnetic resonance imaging at 4 months of age showed bilateral microphthalmia and optic nerve hypoplasia. Appropriate body size was present at 2 years of age, and mental development was favorable. Color fundus photography revealed severe retinal atrophy in both eyes. Electroretinography showed slight responses in the right eye, but no responses in the left eye, suggesting a high risk of blindness. Urinalysis results were normal, creatinine-based estimated glomerular filtration rate was 63.5 mL/min/1.73 m2, and ultrasonography showed bilateral hypoplastic kidneys. Whole exome sequencing revealed de novo frameshift mutations in PAX2 and OPA1. Both variants were classified as pathogenic (PVS1, PS2, PM2) based on the guidelines from the American College of Medical Genetics and Genomics (ACMG). Genetic testing for ocular diseases should be considered for patients with suspected RCS and a high risk of total blindness. [ABSTRACT FROM AUTHOR]
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- 2024
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16. Genome-wide screening reveals the genetic basis of mammalian embryonic eye development
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Chee, Justine M, Lanoue, Louise, Clary, Dave, Higgins, Kendall, Bower, Lynette, Flenniken, Ann, Guo, Ruolin, Adams, David J, Bosch, Fatima, Braun, Robert E, Brown, Steve DM, Chin, H-J Genie, Dickinson, Mary E, Hsu, Chih-Wei, Dobbie, Michael, Gao, Xiang, Galande, Sanjeev, Grobler, Anne, Heaney, Jason D, Herault, Yann, de Angelis, Martin Hrabe, Mammano, Fabio, Nutter, Lauryl MJ, Parkinson, Helen, Qin, Chuan, Shiroishi, Toshi, Sedlacek, Radislav, Seong, J-K, Xu, Ying, Brooks, Brian, McKerlie, Colin, Lloyd, KC Kent, Westerberg, Henrik, and Moshiri, Ala
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Biological Sciences ,Genetics ,Congenital Structural Anomalies ,Rare Diseases ,Human Genome ,Eye Disease and Disorders of Vision ,Pediatric ,2.1 Biological and endogenous factors ,Eye ,Humans ,Mice ,Animals ,Eye Abnormalities ,Anophthalmos ,Microphthalmos ,Coloboma ,Mice ,Knockout ,Embryonic Development ,Phenotype ,Mammals ,MAC spectrum ,Eye development ,Mouse ,IMPC ,Serine-glycine biosynthesis ,CPLANE ,International Mouse Phenotyping Consortium ,Developmental Biology - Abstract
BackgroundMicrophthalmia, anophthalmia, and coloboma (MAC) spectrum disease encompasses a group of eye malformations which play a role in childhood visual impairment. Although the predominant cause of eye malformations is known to be heritable in nature, with 80% of cases displaying loss-of-function mutations in the ocular developmental genes OTX2 or SOX2, the genetic abnormalities underlying the remaining cases of MAC are incompletely understood. This study intended to identify the novel genes and pathways required for early eye development. Additionally, pathways involved in eye formation during embryogenesis are also incompletely understood. This study aims to identify the novel genes and pathways required for early eye development through systematic forward screening of the mammalian genome.ResultsQuery of the International Mouse Phenotyping Consortium (IMPC) database (data release 17.0, August 01, 2022) identified 74 unique knockout lines (genes) with genetically associated eye defects in mouse embryos. The vast majority of eye abnormalities were small or absent eyes, findings most relevant to MAC spectrum disease in humans. A literature search showed that 27 of the 74 lines had previously published knockout mouse models, of which only 15 had ocular defects identified in the original publications. These 12 previously published gene knockouts with no reported ocular abnormalities and the 47 unpublished knockouts with ocular abnormalities identified by the IMPC represent 59 genes not previously associated with early eye development in mice. Of these 59, we identified 19 genes with a reported human eye phenotype. Overall, mining of the IMPC data yielded 40 previously unimplicated genes linked to mammalian eye development. Bioinformatic analysis showed that several of the IMPC genes colocalized to several protein anabolic and pluripotency pathways in early eye development. Of note, our analysis suggests that the serine-glycine pathway producing glycine, a mitochondrial one-carbon donator to folate one-carbon metabolism (FOCM), is essential for eye formation.ConclusionsUsing genome-wide phenotype screening of single-gene knockout mouse lines, STRING analysis, and bioinformatic methods, this study identified genes heretofore unassociated with MAC phenotypes providing models to research novel molecular and cellular mechanisms involved in eye development. These findings have the potential to hasten the diagnosis and treatment of this congenital blinding disease.
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- 2023
17. Zfp503/Nlz2 Is Required for RPE Differentiation and Optic Fissure Closure
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Boobalan, Elangovan, Thompson, Amy H, Alur, Ramakrishna P, McGaughey, David M, Dong, Lijin, Shih, Grace, Vieta-Ferrer, Emile R, Onojafe, Ighovie F, Kalaskar, Vijay K, Arno, Gavin, Lotery, Andrew J, Guan, Bin, Bender, Chelsea, Memon, Omar, Brinster, Lauren, Soleilhavoup, Clement, Panman, Lia, Badea, Tudor C, Minella, Andrea, Lopez, Antonio Jacobo, Thomasy, Sara M, Moshiri, Ala, Blain, Delphine, Hufnagel, Robert B, Cogliati, Tiziana, Bharti, Kapil, and Brooks, Brian P
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Biomedical and Clinical Sciences ,Ophthalmology and Optometry ,Pediatric ,Neurosciences ,Biotechnology ,Genetics ,Eye Disease and Disorders of Vision ,Aetiology ,1.1 Normal biological development and functioning ,2.1 Biological and endogenous factors ,Underpinning research ,Eye ,Animals ,Humans ,Mice ,Coloboma ,Gene Expression Regulation ,Developmental ,Homeodomain Proteins ,Intracellular Signaling Peptides and Proteins ,Melanins ,Mice ,Knockout ,Nerve Tissue Proteins ,Neuropeptides ,Retina ,Retinal Pigment Epithelium ,Zebrafish ,Zfp503 ,NLZ2 ,coloboma ,development ,optic fissure ,Biological Sciences ,Medical and Health Sciences ,Ophthalmology & Optometry ,Ophthalmology and optometry - Abstract
PurposeUveal coloboma is a congenital eye malformation caused by failure of the optic fissure to close in early human development. Despite significant progress in identifying genes whose regulation is important for executing this closure, mutations are detected in a minority of cases using known gene panels, implying additional genetic complexity. We have previously shown knockdown of znf503 (the ortholog of mouse Zfp503) in zebrafish causes coloboma. Here we characterize Zfp503 knockout (KO) mice and evaluate transcriptomic profiling of mutant versus wild-type (WT) retinal pigment epithelium (RPE)/choroid.MethodsZfp503 KO mice were generated by gene targeting using homologous recombination. Embryos were characterized grossly and histologically. Patterns and level of developmentally relevant proteins/genes were examined with immunostaining/in situ hybridization. The transcriptomic profile of E11.5 KO RPE/choroid was compared to that of WT.ResultsZfp503 is dynamically expressed in developing mouse eyes, and loss of its expression results in uveal coloboma. KO embryos exhibit altered mRNA levels and expression patterns of several key transcription factors involved in eye development, including Otx2, Mitf, Pax6, Pax2, Vax1, and Vax2, resulting in a failure to maintain the presumptive RPE, as evidenced by reduced melanin pigmentation and its differentiation into a neural retina-like lineage. Comparison of RNA sequencing data from WT and KO E11.5 embryos demonstrated reduced expression of melanin-related genes and significant overlap with genes known to be dynamically regulated at the optic fissure.ConclusionsThese results demonstrate a critical role of Zfp503 in maintaining RPE fate and optic fissure closure.
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- 2022
18. Embryologische Entwicklung und angeborene Erkrankungen des Auges.
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Bachhuber, Armin
- Abstract
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- 2024
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19. Ocular manifestations of congenital anomalies of the kidney and urinary tract (CAKUT).
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Virth, James, Mack, Heather G., Colville, Deb, Crockett, Emma, and Savige, Judy
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OPTIC nerve abnormalities , *KIDNEY abnormalities , *URINARY organ abnormalities , *CATARACT , *OCULAR manifestations of general diseases , *COLOBOMA , *EYE abnormalities , *GENOMICS , *REFRACTIVE errors , *PHENOTYPES - Abstract
Congenital anomalies of the kidney and urinary tract (CAKUT) are among the most common birth defects worldwide and a major cause of kidney failure in children. Extra-renal manifestations are also common. This study reviewed diseases associated with the Genomics England CAKUT-associated gene panel for ocular anomalies. In addition, each gene was examined for expression in the human retina and an ocular phenotype in mouse models using the Human Protein Atlas and Mouse Genome Informatics databases, respectively. Thirty-four (54%) of the 63 CAKUT-associated genes (55 'green' and 8 'amber') had a reported ocular phenotype. Five of the 6 most common CAKUT-associated genes (PAX2, EYA1, SALL1, GATA3, PBX1) that represent 30% of all diagnoses had ocular features. The ocular abnormalities found with most CAKUT-associated genes and with five of the six commonest were coloboma, microphthalmia, optic disc anomalies, refraction errors (astigmatism, myopia, and hypermetropia), and cataract. Seven of the CAKUT-associated genes studied (11%) had no reported ocular features but were expressed in the human retina or had an ocular phenotype in a mouse model, which suggested further possibly-unrecognised abnormalities. About one third of CAKUT-associated genes (18, 29%) had no ocular associations and were not expressed in the retina, and the corresponding mouse models had no ocular phenotype. Ocular abnormalities in individuals with CAKUT suggest a genetic basis for the disease and sometimes indicate the affected gene. Individuals with CAKUT often have ocular abnormalities and may require an ophthalmic review, monitoring, and treatment to preserve vision. [ABSTRACT FROM AUTHOR]
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- 2024
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20. Retinitis pigmentosa with iris coloboma due to miR‐204 gene variant in a Chinese family
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Zhang Lei, Zhu He‐Lin, Wang Hai‐Yan, Jia Wei, Wang Ru, Cui Zhi‐Li, and Wang Qian‐Feng
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autosomal dominant ,coloboma ,microRNA ,miR‐204 ,retinitis pigmentosa ,Genetics ,QH426-470 - Abstract
Abstract Purpose To characterize the phenotype and genotype of a Chinese family with autosomal‐dominant retinitis pigmentosa (RP) accompanied by iris coloboma. Methods The proband, a 34‐year‐old male, was examined with his family by using fundus photography, optical coherence tomography (OCT), autofluorescence, and full‐field electroretinography (ffERG). Genetic analyses were conducted through whole‐exome sequencing (WES) to screen for variations. Results Three members of this Chinese family were shown to be bilateral iris coloboma. The male proband and his mother exhibited typical RP feature. The proband's late grandfather had been documented manifestation of iris coloboma. The mode of inheritance was confirmed to be autosomal dominance. Through linkage analysis and WES, a heterozygous variation in the miR‐204 gene (n.37C>T), a noncoding RNA gene, was identified in these three members. Conclusions In this third independent and the first Asian family, the existence of a miR‐204 variant associated with RP accompanied by iris coloboma was confirmed. Our findings reinforce the significance of miR‐204 as an important factor influencing visual function in the retina. When phenotypes like RP accompanied by iris coloboma in an autosomal‐dominant pattern, including in Chinese patients, miR‐204 aberrations should be considered.
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- 2024
- Full Text
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21. Congenital Malformations of the Eye: A Pictorial Review and Clinico-Radiological Correlations.
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Guarnera, Alessia, Valente, Paola, Pasquini, Luca, Moltoni, Giulia, Randisi, Francesco, Carducci, Chiara, Carboni, Alessia, Lucignani, Giulia, Napolitano, Antonio, Romanzo, Antonino, Longo, Daniela, Gandolfo, Carlo, and Rossi-Espagnet, Maria Camilla
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RETINA abnormalities , *OPTIC nerve abnormalities , *CATARACT , *CHILD development , *VITREOUS body , *COLOBOMA , *EYE abnormalities , *EYE , *RETROLENTAL fibroplasia , *QUALITY of life , *VISION disorders , *EYE diseases , *CHILDREN ,EYE-socket abnormalities - Abstract
Congenital malformations of the eye represent a wide and heterogeneous spectrum of abnormalities that may be part of a complex syndrome or be isolated. Ocular malformation severity depends on the timing of the causative event during eye formation, ranging from the complete absence of the eye if injury occurs during the first weeks of gestation, to subtle abnormalities if the cause occurs later on. Knowledge of ocular malformations is crucial to performing a tailored imaging protocol and correctly reporting imaging findings. Together with the ophthalmologic evaluation, imaging may help frame ocular malformations and identify underlying genetic conditions. The purpose of this pictorial review is to describe the imaging features of the main ocular malformations and the related ophthalmologic findings in order to provide a clinico-radiological overview of these abnormalities to the clinical radiologist. Sight is a crucial sense for children to explore the world and relate with their parents from birth. Vision impairment or even blindness secondary to ocular malformations deeply affects children's growth and quality of life. [ABSTRACT FROM AUTHOR]
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- 2024
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22. Ocular manifestations of the genetic renal tubulopathies.
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Yang, GeFei, Mack, Heather, Harraka, Philip, Colville, Deb, and Savige, Judy
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OCULAR manifestations of general diseases , *REFRACTIVE errors , *GENETIC disorders , *LABORATORY mice , *REPORTING of diseases - Abstract
The genetic tubulopathies are rare and heterogenous disorders that are often difficult to identify. This study examined the tubulopathy-causing genes for ocular associations that suggested their genetic basis and, in some cases, the affected gene. Sixty-seven genes from the Genomics England renal tubulopathy panel were reviewed for ocular features, and for retinal expression in the Human Protein Atlas and an ocular phenotype in mouse models in the Mouse Genome Informatics database. The genes resulted in disease affecting the proximal tubules (n = 24); the thick ascending limb of the loop of Henle (n = 10); the distal convoluted tubule (n = 15); or the collecting duct (n = 18). Twenty-five of the tubulopathy-associated genes (37%) had ocular features reported in human disease, 49 (73%) were expressed in the retina, although often at low levels, and 16 (24%) of the corresponding mouse models had an ocular phenotype. Ocular abnormalities were more common in genes affected in the proximal tubulopathies (17/24, 71%) than elsewhere (7/43, 16%). They included structural features (coloboma, microphthalmia); refractive errors (myopia, astigmatism); crystal deposition (in oxalosis, cystinosis) and sclerochoroidal calcification (in Bartter, Gitelman syndromes). Retinal atrophy was common in the mitochondrial-associated tubulopathies. Structural abnormalities and crystal deposition were present from childhood, but sclerochoroidal calcification typically occurred after middle age. Ocular abnormalities are uncommon in the genetic tubulopathies but may be helpful in recognizing the underlying genetic disease. The retinal expression and mouse phenotype data suggest that further ocular associations may become apparent with additional reports. Early identification may be necessary to monitor and treat visual complications. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
23. Cleft 8
- Author
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Pellerin, Philippe, Alonso, Nivaldo, da Silva Freitas, Renato, Tonello, Cristiano, Alonso, Nivaldo, editor, Freitas, Renato da Silva, editor, Tonello, Cristiano, editor, and Pellerin, Philippe, editor
- Published
- 2023
- Full Text
- View/download PDF
24. Cleft 9
- Author
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Pellerin, Philippe, Tonello, Cristiano, da Silva Freitas, Renato, Alonso, Nivaldo, Alonso, Nivaldo, editor, Freitas, Renato da Silva, editor, Tonello, Cristiano, editor, and Pellerin, Philippe, editor
- Published
- 2023
- Full Text
- View/download PDF
25. Cleft 10
- Author
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Pellerin, Philippe, Tonello, Cristiano, da Silva Freitas, Renato, Alonso, Nivaldo, Alonso, Nivaldo, editor, Freitas, Renato da Silva, editor, Tonello, Cristiano, editor, and Pellerin, Philippe, editor
- Published
- 2023
- Full Text
- View/download PDF
26. Embryology of Developmental Surgical Disorders of the Posterior Segment
- Author
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Othman, Ihab Saad, Oreaba, Ahmed Hamdy, Özdek, Şengül, editor, Berrocal, Audina, editor, and Spandau, Ulrich, editor
- Published
- 2023
- Full Text
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27. Ophthalmological Surgical Conditions in the Newborn and Neonate
- Author
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Madan, Siddharth, Beri, Sarita, and Saha, Usha, editor
- Published
- 2023
- Full Text
- View/download PDF
28. Clinical characteristics and treatment progress of microphthalmos-anophthalmos-coloboma
- Author
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Bo-Zhao Wang and Yan Cui
- Subjects
microphthalmos ,coloboma ,angle-closure glaucoma ,cataract ,uveal effusion ,Ophthalmology ,RE1-994 - Abstract
Microphthalmos-anophthalmos-coloboma(MAC)is structurally and clinically correlated congenital ocular malformation. Although MAC is relatively rare, they still become an important cause of blindness in children. At present, the etiology of MAC is not clear; a variety of genetic or environmental factors may cause MAC. Because of its special anatomical structure, MAC has complex clinical manifestations and multiple complications. The complications including cataract, angle-closure glaucoma, uveal effusion, retinal detachment, orbital cyst, which are often accompanied with increased risks for surgery and poor prognosis. By summarizing the clinical features, the common types of ocular complications, and the progress of the treatment, this article will enhance clinicians' cognition of MAC and guide clinicians to formulate personalized and safe treatment plans for patients.
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- 2023
- Full Text
- View/download PDF
29. Nasopalpebral Lipoma sine Coloboma Syndrome—First Case Report
- Author
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Ved Prakash Rao Cheruvu, Manal M. Khan, Madhuri Arora, and Vikas Chaudary
- Subjects
abnormalities ,coloboma ,lipoma ,Surgery ,RD1-811 - Abstract
The nasopalpebral lipoma-coloboma syndrome was described for the first time in 1982. It is an autosomal dominant syndrome with complete penetrance and is characterized by features like congenital symmetric upper eyelid and nasopalpebral lipomas, bilateral symmetric upper and lower eyelid colobomas, broad forehead, widow's peak, abnormal eyebrow pattern, telecanthus, broad nasal bridge, maxillary hypoplasia, and ophthalmological abnormalities. We report a case of a milder variant of the nasopalpebral lipoma-coloboma syndrome that we have termed “nasopalpebral lipoma sine coloboma syndrome.” Such a milder variant is not reported hitherto in the literature. We also describe the surgical correction of the deformity in a case that presented in adulthood, with a satisfactory and pleasing aesthetic outcome.
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- 2023
- Full Text
- View/download PDF
30. MIR204 n.37C>T variant as a cause of chorioretinal dystrophy variably associated with iris coloboma, early‐onset cataracts and congenital glaucoma.
- Author
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Jedlickova, Jana, Vajter, Marie, Barta, Tomas, Black, Graeme C. M., Perveen, Rahat, Mares, Jan, Fichtl, Marek, Kousal, Bohdan, Dudakova, Lubica, and Liskova, Petra
- Subjects
- *
CONGENITAL glaucoma , *DYSTROPHY , *CATARACT , *HAPLOTYPES , *ALBINISM - Abstract
Four members of a three‐generation Czech family with early‐onset chorioretinal dystrophy were shown to be heterozygous carriers of the n.37C>T in MIR204. The identification of this previously reported pathogenic variant confirms the existence of a distinct clinical entity caused by a sequence change in MIR204. Chorioretinal dystrophy was variably associated with iris coloboma, congenital glaucoma, and premature cataracts extending the phenotypic range of the condition. In silico analysis of the n.37C>T variant revealed 713 novel targets. Additionally, four family members were shown to be affected by albinism resulting from biallelic pathogenic OCA2 variants. Haplotype analysis excluded relatedness with the original family reported to harbour the n.37C>T variant in MIR204. Identification of a second independent family confirms the existence of a distinct MIR204‐associated clinical entity and suggests that the phenotype may also involve congenital glaucoma. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
31. Achondroplasia with macular coloboma and cone-rod dystrophy: a case report.
- Author
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El-Mofty, Randa M. A. M. and Hassan, Mai M. I.
- Subjects
- *
RETINAL degeneration , *ACHONDROPLASIA , *SHORT stature , *VISUAL acuity , *OSSIFICATION - Abstract
Achondroplasia, an autosomal dominant congenital enchondral ossification, is clinically characterized by short stature, craniofacial, and bone deformities. Ophthalmic features include telecanthus and strabismus; cone-rod dystrophy can also be present. A 12-year-old male presented with decreased vision bilaterally, nystagmus, and achondroplasia. The best corrected visual acuity (BCVA) was Log MAR 1.0 in the right eye and Log MAR 0.8 in the left eye, the anterior segments showed no abnormalities, however the fundus showed bilateral macular coloboma. On electrophysiological assessment, there was also bilateral cone-rod dysfunction. As ophthalmic associations are common in Achondroplasia, thorough ophthalmological examination as well as electrophysiological assessment are mandatory. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
32. Implantable Collamer Lens Subluxation in a Patient with Lenticular Coloboma: A Case Report.
- Author
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Al Alshaikh, Lamees, Bin Helayel, Halah, and Al-Swailem, Samar A.
- Subjects
- *
ANISOMETROPIA , *ASTIGMATISM , *SLIT lamp microscopy , *PATHOLOGY , *PUPILLARY reflex , *CILIARY body , *ACOUSTIC microscopy - Abstract
Objective: Rare coexistence of disease or pathology Background: The efficacy and safety of the implantable collamer lens (ICL) in correcting high astigmatism have been previously reported. They are commonly used as an alternative to laser refractive surgery due to advantages such as leaving the cornea untouched, inducing fewer higher-order aberrations, resulting in better optical and visual quality, and it is a reversible procedure. We aim to present the outcome of ICL in managing anisometropia without cataract in an eye with unilateral lenticular coloboma. Case Report: A 27-year-old man with a Marfanoid body habitus was seeking refractive surgery for the correction of high astigmatism in the right eye. On presentation, the best corrected visual acuity was 20/30 and 20/20 in the right eye and left eye, respectively. Slit lamp examination indicated inferior lens coloboma extending from the 5 o'clock to the 7: 30 o'clock position in the right eye, after dilation of pupil. Following a complete refractive work-up, a toric ICL implantation was the presumed suitable surgery. Three weeks postoperatively, central vaulting was low, his ICL subluxated inferiorly, and the previously implanted temporal footplates were resting over the lenticular defect inferiorly. A high-resolution ultrasound biomicroscopy confirmed the presence of a ciliary body (CB) cyst at 9 o'clock position. Urgent explantation of the unstable ICL was performed. Conclusions: This case report emphasizes the challenges and limitations associated with ICL implantation in patients with lenticular colobomas and coexisting CB cyst. Selecting smaller lenticular colobomas and avoiding direct interaction between the weak zonules area and the ICL haptics are important steps to ensure the stability of implanted lens. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
33. NPHP1‐Related ciliopathies: A new case and major review of the ophthalmic manifestations of 147 reported cases.
- Author
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Reddy, Shivania, Simmers, Russell, Shah, Arth, and Couser, Natario
- Subjects
- *
OCULAR manifestations of general diseases , *GENETIC variation , *HUMAN abnormalities - Abstract
Key Clinical Message: Our case report and review contribute to the understanding of ocular manifestations in NPHP1 ciliopathies by reinforcing the relationship between pathogenic genetic variants and a wide array of ophthalmic abnormalities. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
34. First report of tethered cord syndrome in a patient with Verheij syndrome.
- Author
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Kocaaga, A., Yimenicioglu, S., Atikel, Y. Özdemir, and Yavuz, O. Özkale
- Subjects
- *
GROWTH disorders , *JOINT hypermobility , *TURKS , *PROTEIN structure , *DISABILITIES - Abstract
Verheij syndrome (VRJS) is a rare microdeletion syndrome of chromosome 8q24.3 that is characterized by severe growth retardation, microcephaly, vertebral anomalies, joint laxity/dislocation, psychomotor retardation, cardiac and renal defects, and dysmorphic facial features. Pathogenic variants of PUF60 (Poly-U Binding Splicing Factor 60 kDa) have been found to cause VRJS. Here we present a Turkish patient with Verheij syndrome who has typical facial dysmorphic features and renal and cardiac abnormalities, scoliosis, tethered cord, and mild intellectual disability. This is a case report of a 11-year-old female child who presented with Verheij syndrome. Blood samples were collected from the patient and the family. We performed whole exome sequencing was used to identify potential genetic mutations. We also used 3-dimensional protein structure analysis to identify the effect of the mutation. A de-novo in-frame variant (c.449_457delCAAAGGGGG; p.Ala150_Phe152del) of the PUF60 gene was identified by whole exome sequencing. According to ACMG guidelines in 2015, the mutation is classified as pathogenic and it has been reported in the clinvar database. Results of in-silico prediction software tools predicted the mutation was pathogenic. Protein structure analysis showed that the three residues affected by the in-frame deletion form could lead to impaired stability and function of the PUF60 protein. To date, 25 patients have been reported with PUF60 mutations in the medical literature. In this article, we report a patient with VRJS who had the unusual findings of tethered cord syndrome and renal abnormalities. As far as we know, this is the first patient from Turkey who has been diagnosed with Verheij syndrome. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
35. Feasibility, comparability and outcomes of three acquainted facial island flaps for periorbital defects reconstruction.
- Author
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Fang, Zhuoqun, Wu, Yujie, Li, Jun, Wang, Kejia, He, Ting, Wang, Hongtao, Yang, Xuekang, Liu, Honglei, and Han, Juntao
- Subjects
WOUND healing ,SURGICAL flaps ,PLASTIC surgery ,COLOBOMA ,OCULAR tumors ,RETROSPECTIVE studies ,PATIENT satisfaction ,SURGICAL complications ,TREATMENT effectiveness ,COMPARATIVE studies ,DESCRIPTIVE statistics ,OPHTHALMIC surgery - Abstract
Severe coloboma of ocular malignant neoplasms post‐resection poses a reconstructive challenge to surgeons. To compare the practicability, manipulability and outcomes of temporal (myocutaneous) flaps (TFs), forehead (supratrochlear artery/supraorbital artery) flaps (FFs) and buccal (facial artery) flaps (BFs) for periorbital defects reconstruction, a retrospective case series was conducted and evaluated between March 2014 and March 2021. Patient demographics and clinical parameters including age, gender, pathological diagnosis, operative methods, flap selection, operation time, aesthetic satisfaction and follow‐up period were collected. The differences in complications were compared and assessed of the three flaps, including flap survival, venous congestion and donor site healing. Totally, 68 patients who underwent periorbital reconstructive operations because of common ocular malignant tumours were reviewed in this study. As for aesthetic satisfaction, a score more than "moderately dissatisfied" was obtained in 21 patients with TFs (95.5%), and of which the scores in FFs group were 12 cases (60%) and 16 cases with BFs reconstruction (61.5%) (P <.05). Severe microvascular complications underwent re‐exploration operation occurred in one patient with FFs (1.5%) (P >.05). Notable flap necrosis was observed in two patients with BFs repair (2.9%) and in one case with FFs repair (1.5%), with no statistical difference between the three flap selections (P >.05). Moderate venous congestion occurred in one patient with TFs (1.5%), which was fully meliorated non‐surgically. The three familiar facial island flaps are considered as minor trauma and time‐saving process for reconstructing the extensive periorbital defects with comparable ranks of complications. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
36. Multiple roles for Pax2 in the embryonic mouse eye
- Author
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Bosze, Bernadett, Suarez-Navarro, Julissa, Soofi, Abdul, Lauderdale, James D, Dressler, Gregory R, and Brown, Nadean L
- Subjects
Biomedical and Clinical Sciences ,Ophthalmology and Optometry ,Congenital Structural Anomalies ,Genetics ,Neurosciences ,Eye Disease and Disorders of Vision ,Pediatric ,1.1 Normal biological development and functioning ,Underpinning research ,Neurological ,Eye ,Animals ,Animals ,Genetically Modified ,Body Patterning ,Cell Proliferation ,Coloboma ,Female ,Gene Expression Regulation ,Developmental ,Gene Knock-In Techniques ,Male ,Mice ,Mice ,Inbred C57BL ,Optic Disk ,PAX2 Transcription Factor ,Retina ,Stem Cells ,Pax2 ,Pax6 ,Foxg1 ,RPE ,Optic stalk ,Biological Sciences ,Medical and Health Sciences ,Developmental Biology ,Biological sciences ,Biomedical and clinical sciences ,Health sciences - Abstract
The vertebrate eye anlage grows out of the brain and folds into bilayered optic cups. The eye is patterned along multiple axes, precisely controlled by genetic programs, to delineate neural retina, pigment epithelium, and optic stalk tissues. Pax genes encode developmental regulators of key morphogenetic events, with Pax2 being essential for interpreting inductive signals, including in the eye. PAX2 mutations cause ocular coloboma, when the ventral optic fissure fails to close. Previous studies established that Pax2 is necessary for fissure closure and to maintain the neural retina -- glial optic stalk boundary. Using a Pax2GFP/+ knock-in allele we discovered that the mutant optic nerve head (ONH) lacks molecular boundaries with the retina and RPE, rendering the ONH larger than normal. This was preceded by ventronasal cup mispatterning, a burst of overproliferation and followed by optic cup apoptosis. Our findings support the hypothesis that ONH cells are tripotential, requiring Pax2 to remain committed to glial fates. This work extends current models of ocular development, contributes to broader understanding of tissue boundary formation and informs the underlying mechanisms of human coloboma.
- Published
- 2021
37. A novel pupilloplasty in crescent-shaped suturing pattern for coloboma and traumatic iris defects
- Author
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Xiaoming Yao, Qian Kang, Wei Qi, Yuan Liu, Xiaoping Zhou, Mingwu Wang, Yukun Yang, Fengjiao Zhu, and Wenchao Cao
- Subjects
Iris defect ,Coloboma ,Pupilloplasty ,Crescent ,Ophthalmology ,RE1-994 - Abstract
Abstract Objective Purpose To observe the safety and effect of the C-pupilloplasty for the treatment of iris coloboma and traumatic iris defects. Methods A total of 21 cases (21 eyes) with iris coloboma or traumatic iris defects who underwent C-pupilloplasty (a single-pass three-throw technique) from Feb. 2016 to Mar. 2020 were analyzed retrospectively. Uncorrected visual acuity, refraction, corneal topographic keratometry and endothelial cell density were examined. Results All the patients were successfully treated, and a central and round pupil was restored. The mean follow-up duration was 8.76 ± 3.58 months (ranging from 2 to 14 months). All patients had round or round-like pupils with a diameter less than or equal to 3 mm after the C-pupilloplasty. Very slightly endothelial loss, negligible symptoms such as glare, distortion, dizziness and photophobia were observed. Conclusion We introduced a new technique of pupilloplasty (C-pupilloplasty) which could be a more straight forward and more effective treatment for iris coloboma and traumatic iris defect.
- Published
- 2023
- Full Text
- View/download PDF
38. Exome sequencing in patients with microphthalmia, anophthalmia, and coloboma (MAC) from a consanguineous population
- Author
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Islam, Farrah, Htun, Stephanie, Lai, Li‐Wen, Krall, Max, Poranki, Menitha, Martin, Pierre‐Marie, Sobreira, Nara, Wohler, Elizabeth S, Yu, Jingwei, Moore, Anthony T, and Slavotinek, Anne M
- Subjects
Biological Sciences ,Biomedical and Clinical Sciences ,Genetics ,Clinical Research ,Human Genome ,2.1 Biological and endogenous factors ,Aetiology ,Anophthalmos ,Calcium-Binding Proteins ,Cation Transport Proteins ,Cell Adhesion Molecules ,Coloboma ,Consanguinity ,Exome ,Female ,High-Throughput Nucleotide Sequencing ,Humans ,Kinesins ,Male ,Membrane Proteins ,Microphthalmos ,Mitochondrial Membrane Transport Proteins ,Mutation ,Nerve Tissue Proteins ,Polymorphism ,Single Nucleotide ,Tumor Suppressor Proteins ,Exome Sequencing ,Anophthalmia ,cataract ,CDON ,Microphthalmia ,TENM3 ,Clinical Sciences ,Genetics & Heredity ,Clinical sciences - Abstract
Next-generation sequencing strategies have resulted in mutation detection rates of 21% to 61% in small cohorts of patients with microphthalmia, anophthalmia and coloboma (MAC), but despite progress in identifying novel causative genes, many patients remain without a genetic diagnosis. We studied a cohort of 19 patients with MAC who were ascertained from a population with high rates of consanguinity. Using single nucleotide polymorphism (SNP) arrays and whole exome sequencing (WES), we identified one pathogenic variant in TENM3 in a patient with cataracts in addition to MAC. We also detected novel variants of unknown significance in genes that have previously been associated with MAC, including KIF26B, MICU1 and CDON, and identified variants in candidate genes for MAC from the Wnt signaling pathway, comprising LRP6, WNT2B and IQGAP1, but our findings do not prove causality. Plausible variants were not found for many of the cases, indicating that our current understanding of the pathogenesis of MAC, a highly heterogeneous group of ocular defects, remains incomplete.
- Published
- 2020
39. The impact of genetic testing for microphthalmia, anophthalmia, and coloboma: experiences from a translational approach.
- Author
-
Holt, Richard
- Subjects
OCCUPATIONAL roles ,GENETIC testing ,COLOBOMA ,EYE abnormalities ,INTERPROFESSIONAL relations ,TRANSLATIONAL research ,PHENOTYPES ,MEDICAL coding - Published
- 2023
- Full Text
- View/download PDF
40. NPHP1‐Related ciliopathies: A new case and major review of the ophthalmic manifestations of 147 reported cases
- Author
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Shivania Reddy, Russell Simmers, Arth Shah, and Natario Couser
- Subjects
coloboma ,Joubert syndrome‐4 ,juvenile nephronophthisis‐1 ,NPHP1‐related ciliopathies ,ophthalmology ,senior‐Loken Syndrome‐1 ,Medicine ,Medicine (General) ,R5-920 - Abstract
Key Clinical Message Our case report and review contribute to the understanding of ocular manifestations in NPHP1 ciliopathies by reinforcing the relationship between pathogenic genetic variants and a wide array of ophthalmic abnormalities.
- Published
- 2023
- Full Text
- View/download PDF
41. Doğumsal Retinal Vasküler Anomaliler- 2 (Kolobom, Retinal Kavernöz Hemanjiom, Arteriyo-Venöz Malformasyon, Retinal Kapiller Hemanjioblastom, Von Hippel-Lindau Sendromu).
- Author
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Konuk, Şerife Gülhan and Kılıç, Raşit
- Abstract
Copyright of Current Retina Journal / Güncel Retina Dergisi is the property of Anadolu Kitabevi Basim Yayim Medikal Turizm Kirtasiye Tic. Ltd. Sti. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2023
- Full Text
- View/download PDF
42. Nasopalpebral Lipoma sine Coloboma Syndrome—First Case Report.
- Author
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Cheruvu, Ved Prakash Rao, Khan, Manal M., Arora, Madhuri, and Chaudary, Vikas
- Subjects
- *
SYNDROMES , *EYELIDS , *EYEBROWS , *ADULTS , *HUMAN abnormalities , *LIPOMA - Abstract
The nasopalpebral lipoma-coloboma syndrome was described for the first time in 1982. It is an autosomal dominant syndrome with complete penetrance and is characterized by features like congenital symmetric upper eyelid and nasopalpebral lipomas, bilateral symmetric upper and lower eyelid colobomas, broad forehead, widow's peak, abnormal eyebrow pattern, telecanthus, broad nasal bridge, maxillary hypoplasia, and ophthalmological abnormalities. We report a case of a milder variant of the nasopalpebral lipoma-coloboma syndrome that we have termed "nasopalpebral lipoma sine coloboma syndrome." Such a milder variant is not reported hitherto in the literature. We also describe the surgical correction of the deformity in a case that presented in adulthood, with a satisfactory and pleasing aesthetic outcome. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
43. Insights into the genotype–phenotype relationship of ocular manifestations in Kabuki syndrome.
- Author
-
Shah, Suraj S., Fulton, Anne, Jabroun, Mireille, Brightman, Diana, Simpson, Brittany N., and Bodamer, Olaf A.
- Abstract
We aim to assess if genotype–phenotype correlations are present within ocular manifestations of Kabuki syndrome (KS) among a large multicenter cohort. We conducted a retrospective, medical record review including clinical history and comprehensive ophthalmological examinations of a total of 47 individuals with molecularly confirmed KS and ocular manifestations at Boston Children's Hospital and Cincinnati Children's Hospital Medical Center. We assessed information regarding ocular structural, functional, and adnexal elements as well as pertinent associated phenotypic features associated with KS. For both type 1 KS (KS1) and type 2 KS (KS2), we observed more severe eye pathology in nonsense variants towards the C‐terminus of each gene, KMT2D and KDM6A, respectively. Furthermore, frameshift variants appeared to be not associated with structural ocular elements. Between both types of KS, ocular structural elements were more frequently identified in KS1 compared with KS2, which only involved the optic disc in our cohort. These results reinforce the need for a comprehensive ophthalmologic exam upon diagnosis of KS and regular follow‐up exams. The specific genotype may allow risk stratification of the severity of the ophthalmologic manifestation. However, additional studies involving larger cohorts are needed to replicate our observations and conduct powered analyses to more formally risk‐stratify based on genotype, highlighting the importance of multicenter collaborations in rare disease research. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
44. Simultaneous Requirements for Hes1 in Retinal Neurogenesis and Optic Cup–Stalk Boundary Maintenance
- Author
-
Bosze, Bernadett, Moon, Myung-Soon, Kageyama, Ryoichiro, and Brown, Nadean L
- Subjects
Biomedical and Clinical Sciences ,Ophthalmology and Optometry ,Stem Cell Research - Nonembryonic - Non-Human ,Genetics ,Eye Disease and Disorders of Vision ,Neurosciences ,Stem Cell Research ,1.1 Normal biological development and functioning ,Underpinning research ,Neurological ,Eye ,Animals ,Coloboma ,Ependymoglial Cells ,Gastrulation ,Genetic Association Studies ,Mice ,Mice ,Inbred C57BL ,Mice ,Knockout ,Mice ,Transgenic ,Microphthalmos ,Neurogenesis ,Optic Disk ,Receptors ,Notch ,Retina ,Retinal Bipolar Cells ,Retinal Cone Photoreceptor Cells ,Retinal Ganglion Cells ,Signal Transduction ,Transcription Factor HES-1 ,bHLH ,gliogenesis ,Hes1 ,neurogenesis ,Notch signaling ,retina ,Medical and Health Sciences ,Psychology and Cognitive Sciences ,Neurology & Neurosurgery - Abstract
The bHLH transcription factor Hes1 is a key downstream effector for the Notch signaling pathway. During embryogenesis neural progenitors express low levels of Hes1 in an oscillating pattern, whereas glial brain boundary regions (e.g., isthmus) have high, sustained Hes1 levels that suppress neuronal fates. Here, we show that in the embryonic mouse retina, the optic nerve head and stalk express high Hes1, with the ONH constituting a boundary between the neural retina and glial cells that ultimately line the optic stalk. Using two Cre drivers with distinct spatiotemporal expression we conditionally inactivated Hes1, to delineate the requirements for this transcriptional repressor during retinal neurogenesis versus patterning of the optic cup and stalk. Throughout retinal neurogenesis, Hes1 maintains proliferation and blocks retinal ganglion cell formation, but surprisingly we found it also promotes cone photoreceptor genesis. In the postnatal eye, Hes1 inactivation with Rax-Cre resulted in increased bipolar neurons and a mispositioning of Müller glia. Our results indicate that Notch pathway regulation of cone genesis is more complex than previously assumed, and reveal a novel role for Hes1 in maintaining the optic cup-stalk boundary.SIGNIFICANCE STATEMENT The bHLH repressor Hes1 regulates the timing of neurogenesis, rate of progenitor cell division, gliogenesis, and maintains tissue compartment boundaries. This study expands current eye development models by showing Notch-independent roles for Hes1 in the developing optic nerve head (ONH). Defects in ONH formation result in optic nerve coloboma; our work now inserts Hes1 into the genetic hierarchy regulating optic fissure closure. Given that Hes1 acts analogously in the ONH as the brain isthmus, it prompts future investigation of the ONH as a signaling factor center, or local organizer. Embryonic development of the ONH region has been poorly studied, which is surprising given it is where the pan-ocular disease glaucoma is widely believed to inflict damage on RGC axons.
- Published
- 2020
45. Retinal Lesions Presenting in Childhood
- Author
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Nudleman, Eric, Nagata, Tatsuo, Mukai, Shizuo, Chiang, Michael, Section editor, Albert, Daniel M., editor, Miller, Joan W., editor, Azar, Dimitri T., editor, and Young, Lucy H., editor
- Published
- 2022
- Full Text
- View/download PDF
46. Congenital and Developmental Abnormalities of the Eye, Orbit, and Ocular Adnexa
- Author
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Callahan, Alison B., Robb, Richard M., Chiang, Michael, Section editor, Albert, Daniel M., editor, Miller, Joan W., editor, Azar, Dimitri T., editor, and Young, Lucy H., editor
- Published
- 2022
- Full Text
- View/download PDF
47. Congenital Eyelid Anomalies
- Author
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Katowitz, William R., Katowitz, James A., Steele, Eric, Section editor, Ng, John, Section editor, Albert, Daniel M., editor, Miller, Joan W., editor, Azar, Dimitri T., editor, and Young, Lucy H., editor
- Published
- 2022
- Full Text
- View/download PDF
48. Anophthalmia and Microphthalmia
- Author
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Katowitz, William R., Ben Simon, Guy, editor, Greenberg, Gahl, editor, and Landau Prat, Daphna, editor
- Published
- 2022
- Full Text
- View/download PDF
49. An Overview of Treatment Recommendations for the Treacher Collins Syndrome Patient
- Author
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Yates, David M., Bufford, Sediqua, Yates, David M., editor, and Markiewicz, Michael R., editor
- Published
- 2022
- Full Text
- View/download PDF
50. Ophthalmologic Findings and Reconstruction of Soft Tissue Orbital Deformities: Coloboma and Eyelid Deformities
- Author
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Francis, Ashish, Andhole, Shika, Harshbarger, Raymond, Kelley, Patrick, Amato, Malena M., Yates, David M., editor, and Markiewicz, Michael R., editor
- Published
- 2022
- Full Text
- View/download PDF
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