7 results on '"Chong, W."'
Search Results
2. TRNT1 deficiency: clinical, biochemical and molecular genetic features.
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Wedatilake, Yehani, Niazi, Rojeen, Fassone, Elisa, Powell, Christopher A., Pearce, Sarah, Plagnol, Vincent, Saldanha, José W., Kleta, Robert, Kling Chong, W., Footitt, Emma, Mills, Philippa B., Taanman, Jan-Willem, Minczuk, Michal, Clayton, Peter T., Rahman, Shamima, and Chong, W Kling
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TRANSFER RNA genetics ,NUCLEOTIDYLTRANSFERASES ,ENZYME deficiency ,MITOCHONDRIAL pathology ,ANEMIA ,GENETICS ,COMPARATIVE studies ,DEVELOPMENTAL disabilities ,RESEARCH methodology ,MEDICAL cooperation ,GENETIC mutation ,PROTEINS ,RESEARCH ,RESEARCH funding ,TRANSFER RNA ,EVALUATION research - Abstract
Background: TRNT1 (CCA-adding transfer RNA nucleotidyl transferase) enzyme deficiency is a new metabolic disease caused by defective post-transcriptional modification of mitochondrial and cytosolic transfer RNAs (tRNAs).Results: We investigated four patients from two families with infantile-onset cyclical, aseptic febrile episodes with vomiting and diarrhoea, global electrolyte imbalance during these episodes, sideroblastic anaemia, B lymphocyte immunodeficiency, retinitis pigmentosa, hepatosplenomegaly, exocrine pancreatic insufficiency and renal tubulopathy. Other clinical features found in children include sensorineural deafness, cerebellar atrophy, brittle hair, partial villous atrophy and nephrocalcinosis. Whole exome sequencing and bioinformatic filtering were utilised to identify recessive compound heterozygous TRNT1 mutations (missense mutation c.668T>C, p.Ile223Thr and a novel splice mutation c.342+5G>T) segregating with disease in the first family. The second family was found to have a homozygous TRNT1 mutation (c.569G>T), p.Arg190Ile, (previously published). We found normal mitochondrial translation products using passage matched controls and functional perturbation of 3' CCA addition to mitochondrial tRNAs (tRNA(Cys), tRNA(LeuUUR) and tRNA(His)) in fibroblasts from two patients, demonstrating a pathomechanism affecting the CCA addition to mt-tRNAs. Acute management of these patients included transfusion for anaemia, fluid and electrolyte replacement and immunoglobulin therapy. We also describe three-year follow-up findings after treatment by bone marrow transplantation in one patient, with resolution of fever and reversal of the abnormal metabolic profile.Conclusions: Our report highlights that TRNT1 mutations cause a spectrum of disease ranging from a childhood-onset complex disease with manifestations in most organs to an adult-onset isolated retinitis pigmentosa presentation. Systematic review of all TRNT1 cases and mutations reported to date revealed a distinctive phenotypic spectrum and metabolic and other investigative findings, which will facilitate rapid clinical recognition of future cases. [ABSTRACT FROM AUTHOR]- Published
- 2016
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3. Congenital hypopituitarism: clinical, molecular and neuroradiological correlates.
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Mehta, Ameeta, Hindmarsh, Peter C., Mehta, Hiten, Turton, James P. G., Russell-Eggitt, Isabelle, Taylor, David, Chong, W. K., and Dattani, Mehul T.
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GENETIC mutation ,SHEEHAN'S syndrome ,PITUITARY hormones ,MAGNETIC resonance imaging ,CORPUS callosum - Abstract
Objective Recent studies have suggested that mutations in genes encoding several hypothalamo–pituitary (H–P) transcription factors result in hypopituitarism [isolated GH deficiency (IGHD) and combined pituitary hormone deficiency (CPHD)], which may in turn be related to the neuroanatomy revealed by magnetic resonance (MR) imaging. Although studies have focused on patients with either optic nerve hypoplasia (ONH) or isolated hypopituitarism with normal optic nerves, few studies have compared the two groups. We aimed to relate the clinical phenotype of a large cohort ( n = 170) of children with congenital hypopituitarism including septo-optic dysplasia (SOD) attending a single centre to the neuroradiological and genetic findings. Design Clinical, biochemical, MR imaging and molecular data were analysed retrospectively in 170 patients with or ‘at-risk’ (with ONH) of hypopituitarism to determine predictors of hypopituitarism. Results The presence of ONH was significantly associated with an absent septum pellucidum [odds ratio (OR) 31·5, 95% confidence intervals (CI) 7·3–136·6, P < 0·001], an abnormal corpus callosum (OR 10·5, 95% CI 3·8–28·6, P < 0·001) and stalk abnormalities (OR 2·3, 95% CI 1·2–4·2, P = 0·009). The risk of hypopituitarism was 27·2 times greater in patients with an undescended posterior pituitary (95% CI 3·6–205·1, P < 0·001). Anterior pituitary hypoplasia (OR 3·1, 95% CI 1·3–7·0, P = 0·006) and an absent pituitary stalk ( P < 0·001) were also significantly associated with hypopituitarism. With respect to the type or severity of hypopituitarism, CPHD was more often associated with an abnormal corpus callosum (OR 6·1, 95% CI 1·4–27·4, P = 0·008) and stalk abnormalities (OR 2·8, 95% CI 1·3–6·1, P = 0·006). Male to female ratio was significantly greater in patients with normal optic nerves (3·3:1) as compared with those with ONH (1·2:1). The prevalence of diabetes insipidus, thyrotrophin and ACTH deficiencies was significantly greater in patients with ONH as compared with ‘idiopathic’ hypopituitarism. Mutations in pituitary transcription factors and genes regulating GH secretion were rare (5/170) in this cohort of patients with sporadic hypopituitarism. Conclusion Our data suggest that individuals presenting with ONH are at high risk for neuroradiologic and endocrine abnormalities. The neuroradiologic features are predictive not only of the presence, but also of the type, of hypopituitarism. The association of midline abnormalities with hypopituitarism in this cohort suggests a common developmental origin for these features, the aetiology of which remains unidentified in the majority of cases. [ABSTRACT FROM AUTHOR]
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- 2009
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4. Mutations at the BLK locus linked to maturity onset diabetes of the young and β-cell dysfunction.
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Borowiec, Maciej, Liew, Chong W., Thompson, Ryan, Boonyasrisawat, Watip, Jiang Hu, Mlynarski, Wojciech M., El Khattabi, Ilham, Sung-Hoon Kim, Marselli, Lorella, Rich, Stephen S., Krolewski, Andrzej S., Bonner-Weir, Susan, Sharma, Arun, Sale, Michele, Mychaleckyj, Josyf C., Kulkarni, Rohit N., and Doria, Alessandro
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GENETICS ,GENETIC mutation ,TRANSCRIPTION factors ,BIOLOGICAL research ,CELL physiology ,CYTOLOGICAL research - Abstract
Maturity-onset diabetes of the young (MODY) is a subtype of diabetes defined by an autosomal pattern of inheritance and a young age at onset, often before age 25. MODY is genetically heterogeneous, with 8 distinct MODY genes identified to date and more believed to exist. We resequenced 732 kb of genomic sequence at 8p23 in 6 MODY families unlinked to known MODY genes that showed evidence of linkage at that location. Of the 410 sequence differences that we identified, 5 had a frequency <1% in the general population and segregated with diabetes in 3 of the families, including the 2 showing the strongest support for linkage at this location. The 5 mutations were all placed within 100 kb corresponding to the BLK gene. One resulted in an Ala71Thr substitution; the other 4 were noncoding and determined decreased in vitro promoter activity in reporter gene experiments. We found that BLK—a nonreceptor tyrosine-kinase of the src family of proto-oncogenes—is expressed in β-cells where it enhances insulin synthesis and secretion in response to glucose by up-regulating transcription factors Pdx1 and Nkx6.1. These actions are greatly attenuated by the Ala71Thr mutation. These findings point to BLK as a previously unrecognized modulator of β-cell function, the deficit of which may lead to the development of diabetes. [ABSTRACT FROM AUTHOR]
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- 2009
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5. Pyridoxine-dependent seizures: a family phenotype that leads to severe cognitive deficits, regardless of treatment regime.
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Rankin, Peter, Harrison, Sue, Chong, W. K., Boyd, Stewart, and Aylett, Sarah E.
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VITAMIN B6 ,GENETIC mutation ,NEUROPSYCHOLOGICAL tests ,LEARNING disabilities ,COGNITION disorders - Abstract
The neuropsychological and clinical histories of three male siblings affected by pyridoxine-dependent seizures with known homozygous antiquitin mutations are presented. Neuropsychological evaluation is reported from when the siblings were 11, 9, and 7 years of age. Two of the siblings had received early pyridoxine treatment (antenatal, 2–4wks into pregnancy) and one had received late treatment (2mo postnatal). However, there was no differential effect on cognitive outcome, with all three siblings having moderate to severe learning disability. Unlike previously reported cases that received early postnatal treatment, none of the siblings had relatively preserved non-verbal cognitive skills. Equally, their intellectual performance over time did not increase above the 1st centile despite high maintenance doses of vitamin B6 (range 16–26mg/kg/d), and mild sensory neuropathy was reported on nerve conduction studies. The findings in these siblings challenge assumptions that early and high dose pyridoxine treatment can benefit cognition in this population and suggest routine electromyography monitoring may be beneficial. [ABSTRACT FROM AUTHOR]
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- 2007
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6. Pantothenate kinase 2 mutation with classic pantothenate-kinase-associated neurodegeneration without 'eye-of-the-tiger' sign on MRI in a pair of siblings.
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Zolkipli, Zarazuela, Dahmoush, Hisham, Saunders, Dawn E., Chong, W. K. Kling, and Surtees, Robert
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GENETIC mutation ,MAGNETIC resonance imaging ,MEDICAL imaging systems ,DIAGNOSTIC imaging ,DYSTONIA ,GENETICS ,IRON metabolism ,BASAL ganglia ,BRAIN stem ,SIBLINGS ,TRANSFERASES - Abstract
It has been postulated that all patients with pantothenate kinase 2 (PANK2) mutations causing pantothenate-kinase-associated neurodegeneration (PKAN) are associated with the 'eye-of-the-tiger' sign on MRI. We report a pair of siblings who presented with dystonia and who have been found to be homozygous for 104C>A, S35X mutation, confirming the diagnosis of PKAN. They do not have the typical iron deposition in the globi pallida or substantia nigra on MR imaging. [ABSTRACT FROM AUTHOR]
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- 2006
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7. Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans.
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Kelberman, Daniel, Rizzoti, Karine, Avilion, Ariel, Bitner-Glindzicz, Maria, Cianfarani, Stefano, Collins, Julie, Chong, W. Kling, Kirk, Jeremy M. W., Achermann, John C., Ross, Richard, Carmignac, Danielle, Lovell-Badge, Robin, Robinson, Iain C. A. F., and Dattani, Mehul T.
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GENETIC mutation , *TRANSCRIPTION factors , *SOMATOTROPIN , *LUTEINIZING hormone , *GLYCOPROTEIN hormones , *EMBRYOLOGY , *ANIMAL experimentation , *COMPARATIVE studies , *EYE abnormalities , *HYPOTHALAMUS , *MICE , *PITUITARY gland , *PROTEINS , *RESEARCH funding , *DNA-binding proteins , *MULTIPLE human abnormalities - Abstract
The transcription factor SOX2 is expressed most notably in the developing CNS and placodes, where it plays critical roles in embryogenesis. Heterozygous de novo mutations in SOX2 have previously been associated with bilateral anophthalmia/microphthalmia, developmental delay, short stature, and male genital tract abnormalities. Here we investigated the role of Sox2 in murine pituitary development. Mice heterozygous for a targeted disruption of Sox2 did not manifest eye defects, but showed abnormal anterior pituitary development with reduced levels of growth hormone, luteinizing hormone, and thyroid-stimulating hormone. Consequently, we identified 8 individuals (from a cohort of 235 patients) with heterozygous sequence variations in SOX2. Six of these were de novo mutations, predicted to result in truncated protein products, that exhibited partial or complete loss of function (DNA binding, nuclear translocation, or transactivation). Clinical evaluation revealed that, in addition to bilateral eye defects, SOX2 mutations were associated with anterior pituitary hypoplasia and hypogonadotropic hypogonadism, variable defects affecting the corpus callosum and mesial temporal structures, hypothalamic hamartoma, sensorineural hearing loss, and esophageal atresia. Our data show that SOX2 is necessary for the normal development and function of the hypothalamo-pituitary and reproductive axes in both humans and mice. [ABSTRACT FROM AUTHOR]
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- 2006
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