18 results on '"Meinecke, P."'
Search Results
2. Recurrent fusions in PLAGL1 define a distinct subset of pediatric-type supratentorial neuroepithelial tumors.
- Author
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Sievers P, Henneken SC, Blume C, Sill M, Schrimpf D, Stichel D, Okonechnikov K, Reuss DE, Benzel J, Maaß KK, Kool M, Sturm D, Zheng T, Ghasemi DR, Kohlhof-Meinecke P, Cruz O, Suñol M, Lavarino C, Ruf V, Boldt HB, Pagès M, Pouget C, Schweizer L, Kranendonk MEG, Akhtar N, Bunkowski S, Stadelmann C, Schüller U, Mueller WC, Dohmen H, Acker T, Harter PN, Mawrin C, Beschorner R, Brandner S, Snuderl M, Abdullaev Z, Aldape K, Gilbert MR, Armstrong TS, Ellison DW, Capper D, Ichimura K, Reifenberger G, Grundy RG, Jabado N, Krskova L, Zapotocky M, Vicha A, Varlet P, Wesseling P, Rutkowski S, Korshunov A, Wick W, Pfister SM, Jones DTW, von Deimling A, Pajtler KW, and Sahm F
- Subjects
- Child, Female, Humans, Male, Oncogene Fusion, Cell Cycle Proteins genetics, Ependymoma genetics, Supratentorial Neoplasms genetics, Transcription Factors genetics, Tumor Suppressor Proteins genetics
- Abstract
Ependymomas encompass a heterogeneous group of central nervous system (CNS) neoplasms that occur along the entire neuroaxis. In recent years, extensive (epi-)genomic profiling efforts have identified several molecular groups of ependymoma that are characterized by distinct molecular alterations and/or patterns. Based on unsupervised visualization of a large cohort of genome-wide DNA methylation data, we identified a highly distinct group of pediatric-type tumors (n = 40) forming a cluster separate from all established CNS tumor types, of which a high proportion were histopathologically diagnosed as ependymoma. RNA sequencing revealed recurrent fusions involving the pleomorphic adenoma gene-like 1 (PLAGL1) gene in 19 of 20 of the samples analyzed, with the most common fusion being EWSR1:PLAGL1 (n = 13). Five tumors showed a PLAGL1:FOXO1 fusion and one a PLAGL1:EP300 fusion. High transcript levels of PLAGL1 were noted in these tumors, with concurrent overexpression of the imprinted genes H19 and IGF2, which are regulated by PLAGL1. Histopathological review of cases with sufficient material (n = 16) demonstrated a broad morphological spectrum of tumors with predominant ependymoma-like features. Immunohistochemically, tumors were GFAP positive and OLIG2- and SOX10 negative. In 3/16 of the cases, a dot-like positivity for EMA was detected. All tumors in our series were located in the supratentorial compartment. Median age of the patients at the time of diagnosis was 6.2 years. Median progression-free survival was 35 months (for 11 patients with data available). In summary, our findings suggest the existence of a novel group of supratentorial neuroepithelial tumors that are characterized by recurrent PLAGL1 fusions and enriched for pediatric patients., (© 2021. The Author(s).)
- Published
- 2021
- Full Text
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3. An unusual combination of EEC syndrome and hypomelanosis Ito due to a p63 mutation.
- Author
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Lehmann K, Mundlos S, and Meinecke P
- Subjects
- Abnormalities, Multiple diagnosis, Child, Preschool, Cleft Lip genetics, Cleft Palate genetics, DNA-Binding Proteins, Ectodermal Dysplasia diagnosis, Exons genetics, Genes, Tumor Suppressor, Hand Deformities, Congenital diagnosis, Humans, Male, Pigmentation Disorders complications, Pigmentation Disorders diagnosis, Syndrome, Transcription Factors, Tumor Suppressor Proteins, Abnormalities, Multiple genetics, Ectodermal Dysplasia genetics, Hand Deformities, Congenital genetics, Mutation, Missense, Phosphoproteins genetics, Pigmentation Disorders genetics, Trans-Activators genetics
- Published
- 2005
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4. Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8.
- Author
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Lüdecke HJ, Schmidt O, Nardmann J, von Holtum D, Meinecke P, Muenke M, and Horsthemke B
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- Child, Chromosome Breakage genetics, Contig Mapping, Cosmids, Electrophoresis, Gel, Pulsed-Field, Expressed Sequence Tags, Female, Gene Deletion, Humans, In Situ Hybridization, Fluorescence, Karyotyping, Male, Polymerase Chain Reaction, Chromosomes, Human, Pair 8 genetics, Langer-Giedion Syndrome genetics
- Abstract
The tricho-rhino-phalangeal syndrome type II (TRPS II, or Langer-Giedion syndrome) is an example of contiguous gene syndromes, as it comprises the clinical features of two autosomal dominant diseases, TRPS I and a form of multiple cartilaginous exostoses caused by mutations in the EXT1 gene. We have constructed a contig of cosmid, lambda-phage, PAC, and YAC clones, which covers the entire TRPS I critical region. Using these clones we identified a novel submicroscopic deletion in a TRPS I patient and refined the proximal border of the minimal TRPS1 gene region by precisely mapping the inversion breakpoint of another patient. As a first step towards a complete inventory of genes in the Langer-Giedion syndrome chromosome region (LGCR) with the ultimate aim to identify the TRPS1 gene, we analyzed 23 human expressed sequence tags (ESTs) and four genes (EIF3S3, RAD21, OPG, CXIV) which had been assigned to human 8q24.1. Our analyses indicate that the LGCR is gene-poor, because none of the ESTs and genes map to the minimal TRPS1 gene region and only two of these genes, RAD21 and EIF3S3, are located within the shortest region of deletion overlap of TRPS II patients. Two genes, OPG and CXIV, which are deleted only in some patients with TRPS II may contribute to the clinical variability of this syndrome.
- Published
- 1999
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5. The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients.
- Author
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Schrander-Stumpel C, Meinecke P, Wilson G, Gillessen-Kaesbach G, Tinschert S, König R, Philip N, Rizzo R, Schrander J, and Pfeiffer L
- Subjects
- Adolescent, Child, Child, Preschool, Dermatoglyphics, Female, Humans, Infant, Japan, Male, Phenotype, Syndrome, Abnormalities, Multiple ethnology, Abnormalities, Multiple genetics, Face abnormalities, Intellectual Disability ethnology, Intellectual Disability genetics
- Abstract
The Kabuki (Niikawa-Kuroki) syndrome was reported in 1981 by Niikawa et al. and Kuroki et al. in a total of ten unrelated Japanese children with a characteristic array of multiple congenital anomalies and mental retardation. The syndrome is characterized by a distinct face, mild to moderate mental retardation, postnatal growth retardation, dermatoglyphic and skeletal abnormalities. In Japan, the syndrome appears to have an incidence of about 1:32,000 newborns. Outside of Japan, a growing number of patients have been recognized. Clinical data are presented on 29 Caucasian patients; the patients were diagnosed over a relatively short period of time, indicating that the incidence outside of Japan is probably not lower than in Japan. A literature review of 89 patients (60 Japanese and 29 non-Japanese) is given. In 66% of the non-Japanese patients serious neurological problems were present, most notably hypotonia and feeding problems (which were not only related to the cleft palate); this was not reported in the Japanese patients. Inheritance is not clear. Most patients are isolated, sex-ratio is equal. The syndrome can be recognized in patients with cleft (lip/)palate, with mild to moderate developmental delay and in young children with hypotonia and/or feeding problems. In counselling parents, the designation "Kabuki" syndrome seems to be more appropriate than "Kabuki make-up" syndrome.
- Published
- 1994
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6. [CHILD syndrome. Case report of a rare genetic dermatosis].
- Author
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Peter C and Meinecke P
- Subjects
- Biopsy, Female, Humans, Ichthyosis diagnosis, Ichthyosis pathology, Infant, Nevus, Pigmented diagnosis, Nevus, Pigmented pathology, Polydactyly diagnosis, Polydactyly genetics, Polydactyly pathology, Sex Chromosome Aberrations genetics, Skin pathology, Skin Neoplasms diagnosis, Skin Neoplasms pathology, Syndrome, X Chromosome, Ichthyosis genetics, Nevus, Pigmented genetics, Skin Neoplasms genetics
- Abstract
We report on a 2-month-old girl who developed unilateral ichthyosiform erythrodermia on the right side of her trunk and the right leg 1 week after birth. In addition, there was hexadactyly of her right hand. Apart from that, close physical examinations did not reveal any other defects. We diagnosed this condition as CHILD syndrome (congenital hemidysplasia with ichthyosiform nevus and limb defects).
- Published
- 1993
7. [FG syndrome in 2 half brothers].
- Author
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Wieg C and Meinecke P
- Subjects
- Adult, Child, Preschool, Female, Humans, Male, Abnormalities, Multiple genetics, Intellectual Disability genetics, Sex Chromosome Aberrations genetics, X Chromosome
- Abstract
We report on two half-brothers with the FG syndrome which is an X-linked recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome. Both patients show postnatal short stature and an altogether characteristic face consisting of droopy appearance, macrocephaly, frontal upsweep, hypertelorism, full lower lip, retrognathia, and dysmorphic ears. Moreover, since early infancy both have a tendency towards constipation, their muscle tone is low and psychomotor development is moderately retarded. Minor expression of this syndrome in the patients' mother and her two mentally retarded brothers give additional support to the X-linked nature of the condition. On the basis of the pertinent literature, a concise description of this MCA/MR syndrome with variable expression is given. Diagnostic evaluation of dysmorphic male patients with psychomotor retardation should always consider the FG syndrome which has been known since 1974 but still is inadequately recognised in the German literature.
- Published
- 1991
8. Further delineation of the ichthyosis follicularis, atrichia, and photophobia syndrome.
- Author
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Hamm H, Meinecke P, and Traupe H
- Subjects
- Alopecia pathology, Humans, Infant, Male, Syndrome, Alopecia congenital, Ichthyosis pathology, Light
- Abstract
We describe an 18-month-old male infant suffering from the ichthyosis follicularis, atrichia, and photophobia (IFAP) syndrome and further delineate the clinical phenotype. Severe retardation of growth and psychomotor development, chill-like seizures, bronchial asthma, urticaria, a proneness to skin infections and transient nail dystrophy observed in our patient are non-obligatory manifestations of this disorder. Histological examination of the atrichia revealed poorly developed, shortened hair follicles and a complete absence of sebaceous glands. The sex ratio of published cases suggests an X-linked recessive inheritance. The marked clinical variability of the IFAP syndrome might be the expression of a contiguous gene defect.
- Published
- 1991
- Full Text
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9. [Brachmann-de Lange syndrome in 16 of our patients].
- Author
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Pankau R, Johannson W, and Meinecke P
- Subjects
- Adolescent, Child, Child Development, Child, Preschool, De Lange Syndrome genetics, Female, Follow-Up Studies, Humans, Infant, Infant, Newborn, Karyotyping, Male, De Lange Syndrome diagnosis
- Abstract
The Brachmann-de Lange-syndrome (Cornelia de Lange-syndrome) belongs to the group of well established multiple congenital anomalies/mental retardation syndromes. The main features are a characteristic dysmorphic face, short stature, defects mainly of the upper limbs and severe psychomotor retardation. A variety of internal anomalies belongs to the non obligatory features of the syndrome. Based on 16 own observations (7 females, 9 males) aged between 1 day and 16 years, we describe the clinical variability of the Brachmann-de Lange-syndrome. Relatively poor prognosis is shown by the fact that up to now 6 of the patients have died.
- Published
- 1990
10. [Hypertelorism-hypospadias (BBB) syndrome. 2 additional family studies].
- Author
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Krause M, Meinecke P, Krins M, and Grote W
- Subjects
- Cleft Lip genetics, Cleft Palate genetics, Diagnosis, Differential, Humans, Infant, Karyotyping, Male, Sex Chromosome Aberrations genetics, Syndrome, X Chromosome, Bone Diseases, Developmental genetics, Hypertelorism genetics, Hypospadias genetics
- Abstract
We report on two unrelated families with the hypertelorism-hypospadias (BBB-) syndrome. The male index patients, 3 and 10 months old, respectively, have ocular hypertelorism, cleft lip and palate, high and broad nasal bridge and hypospadias. The patients' mothers, maternal grandmothers and one patient's sister show hypertelorism. In addition, we summarize the characteristics of previously published cases.
- Published
- 1990
11. [Abnormalities-retardation syndrome caused by incomplete triploidy].
- Author
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Meinecke P and Engelbrecht R
- Subjects
- Child, Preschool, Chromosome Disorders, Humans, Karyotyping, Male, Syndrome, Abnormalities, Multiple genetics, Chromosome Aberrations genetics, Intellectual Disability genetics, Ploidies
- Abstract
We report on a four year old boy with multiple congenital anomalies and mental retardation due to incomplete triploidy (diploid triploid mixoploidy). Initially, we had thought of the Silver-Russell syndrome. The main characteristics in the patient are short stature, body asymmetry, hypogenitalism, and considerable mental retardation. In addition, there are several minor anomalies of the hands and feet. The diagnosis was verified by microscopic detection of a triploid cell line in cultivated skin fibroblasts and by supplementary studies using flow cytometry. The characteristics of this recognizable multiple congenital anomalies/mental retardation syndrome are discussed with reference to the pertinent literature. As differential diagnosis, in particular the Silver-Russell syndrome has to be taken into account.
- Published
- 1988
12. The Weaver syndrome in a girl.
- Author
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Meinecke P, Schaefer E, and Engelbrecht R
- Subjects
- Bone Development, Face abnormalities, Female, Humans, Infant, Syndrome, Gigantism diagnosis
- Abstract
This paper reports the first female case of the Weaver syndrome. The prominent clinical features are gigantism, macrocephaly, and the characteristic facial dysmorphism. Hypertonia and bone maturation acceleration are somewhat less pronounced than in the formerly published cases of male patients. The etiology of the syndrome remains unclear, but if genetic, X-linked recessive inheritance can be excluded.
- Published
- 1983
- Full Text
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13. [Cerebro-costo-mandibular syndrome without cerebral involvement in a 4-year-old boy].
- Author
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Meinecke P, Wolff G, and Schaefer E
- Subjects
- Child, Preschool, Cleft Palate genetics, Humans, Male, Micrognathism genetics, Syndrome, Cleft Palate diagnosis, Micrognathism diagnosis, Ribs abnormalities, Tongue abnormalities
- Abstract
In a four year old boy the combination of Robin sequence and multiple dorsal rib defects on the first day of life could be classified as cerebro-costo-mandibular syndrome. In contrast to an unfavorable clinical course with cerebral involvement which has repeatedly been observed, in our patient psychomotor development has been normal so far. A brief literature review of a total of 36 patients shows that despite a unfavorable prognosis quoad vitam, roughly half the patients have survived. Half of the surviving patients showed functional disorders of the central nervous system, and only one third was mentally retarded. The favorable clinical course documented here thus supports the hypothesis that cerebral symptoms are not an obligatory component of the syndrome, but are only to be regarded as a facultative risk in the "costo-mandibular" syndrome. Accordingly, therapeutic nihilism does not seem to be justified. The etiology of the cerebro-costo-mandibular syndrome could not be clarified unequivocally up to now. A series of family observations indicate a monogenic cause, but genetic heterogeneity can not be ruled out.
- Published
- 1987
14. [Coffin-Siris syndrome in a 5-year-old girl].
- Author
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Meinecke P, Engelbrecht R, and Schaefer E
- Subjects
- Child, Preschool, Female, Fingers abnormalities, Humans, Hypertrichosis diagnosis, Nails, Malformed, Patella abnormalities, Syndrome, Abnormalities, Multiple diagnosis, Intellectual Disability diagnosis
- Abstract
A 5 1/2 year old female patient with Coffin-Siris syndrome is described. This syndrome is characterised by multiple congenital anomalies and mental retardation. The important clinical features include postnatal growth retardation, microcephaly, considerable psychomotor retardation, coarse facies with thick lips, sparse scalp hair with hypertrichosis of the face and body, as well as hypoplasia or even aplasia of distal phalanges of fingers and toes. Chromosomal aberrations, which could be considered as differential diagnosis are excluded by the finding of a normal karyotype. The aetiology or pathogenesis of this syndrome are not really known.
- Published
- 1986
15. [Knee pterygium syndrome in a newborn infant].
- Author
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Meinecke P, Menzel J, and Froster-Iskenius U
- Subjects
- Cleft Lip genetics, Cleft Palate genetics, Humans, Infant, Newborn, Male, Nails, Malformed, Scrotum abnormalities, Syndactyly genetics, Syndrome, Thumb abnormalities, Abnormalities, Multiple genetics, Knee abnormalities, Pterygium genetics
- Abstract
We report on a newborn boy with popliteal pterygium syndrome. Congenital anomalies included popliteal pterygia, symblepharon, cleft lip and palate with syngnathia, severe hypoplasia of both thumbs, a characteristic nail anomaly of both first toes, multiple syndactylies, and a hypoplastic scrotum with cryptorchidism. Mental development can be expected to be normal. Overall prognosis of the disorder after detailed operative correction is apparently favorable. Differential diagnosis is discussed in detail. The syndrome is autosomal dominantly inherited, our patient represents an isolated case.
- Published
- 1989
16. The velo-cardio-facial (Shprintzen) syndrome. Clinical variability in eight patients.
- Author
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Meinecke P, Beemer FA, Schinzel A, and Kushnick T
- Subjects
- Abnormalities, Multiple pathology, Adult, Cleft Palate pathology, Female, Heart Defects, Congenital pathology, Humans, Infant, Newborn, Intellectual Disability pathology, Male, Nasolacrimal Duct abnormalities, Syndrome, Tetralogy of Fallot pathology, Abnormalities, Multiple genetics, Cleft Palate genetics, Heart Defects, Congenital genetics, Intellectual Disability genetics
- Abstract
Eight patients (three sporadic, five from two families) with the velo-cardio-facial syndrome (VCFS) or Shprintzen syndrome are reported. Major clinical findings of this syndrome include a characteristic pattern of facial dysmorphisms, cleft palate, cardio-vascular malformations, and (mostly mild-to-moderate) mental retardation or learning difficulties. The syndrome probably is caused by a dominant gene with very variable expression. From previous reports mostly ascertained from cardio-vascular or cleft palate clinics, the incidence of cleft palate and heart defects was calculated to be 98% and 82%, respectively. Out of eight patients of this study who were diagnosed mainly through their pattern of facial dysmorphisms, only two and four had clefts and heart defects, respectively, further demonstrating the variability in the expression of this gene. Similarly, mental retardation, noted in 100% of previous publications, was not present in all of our patients. In two instances, examination of the mother revealed that she probably carried the mutant gene, but that she showed a milder clinical expression than the index patient. It is suggested that careful family investigations should be performed following detection of an index patient, and that the rate of fresh mutations might be not as high as previously assumed.
- Published
- 1986
- Full Text
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17. [Wiedemann-Beckwith syndrome. Study of an oligosymptomatic form].
- Author
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Lemke J, Meinecke P, and Frank HD
- Subjects
- Abnormalities, Multiple genetics, Diagnosis, Differential, Humans, Infant, Newborn, Male, Syndrome, Gigantism genetics, Hernia, Umbilical genetics, Macroglossia genetics
- Abstract
An infant with an incomplete expression of Wiedemann-Beckwith syndrome during the neonatal period was suspected to suffer from hypothyroidism. However, after exclusion of this tentative diagnosis the phenotypic characteristics lead to the correct diagnosis. In addition to the macroglossia, the typical facial signs of this syndrome such as capillary haemangioma of the glabella, soft tissue folds under the eyes and linear indentations of the ear lobes are demonstrable. Gigantism and umbilical hernia are absent. A tendency to hypoglycaemia and the increased risk of malignancy are the important aspects of this syndrome, which may be expressed in a variety of clinical forms. So far the aetiology of this syndrome is unknown although familial cases implicate the involvement of genetic factors.
- Published
- 1986
18. Compositional analysis of collagen from patients with diverse forms of osteogenesis imperfecta.
- Author
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Kirsch E, Krieg T, Nerlich A, Remberger K, Meinecke P, Kunze D, and Müller PK
- Subjects
- Adolescent, Adult, Child, Child, Preschool, Fibroblasts metabolism, Humans, Hydroxylysine metabolism, Infant, Newborn, Lysine metabolism, Skin metabolism, Collagen metabolism, Osteogenesis Imperfecta metabolism
- Abstract
Collagen was extracted by pepsin treatment from various tissues and skin fibroblasts of 23 patients belonging to different types of osteogenesis imperfecta (OI), and characterized by molecular sieve and ion exchange chromatography, gel electrophoresis, and amino acid analysis. We found an elevated collagen III/I ratio in the skin of one patient with OI type I but almost normal values in skin fibroblasts of two other patients of this OI type. Five patients with OI type II had a normal collagen III/I ratio in their skin and skin fibroblasts, but the degree of hydroxylation of lysine residues in collagen I and III from their skin, bone, calvarium, and noncalcified calvarial tissue was increased. Patients belonging to OI types II, III, and IV had also considerable amounts of collagen III in their long bones, while bone tissue from controls contained only type I collagen. The content of type V in calcified tissues was virtually the same in controls and patients.
- Published
- 1987
- Full Text
- View/download PDF
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