Goltz–Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap
| Autor: | Kerstin Kutsche, Dagmar Wieczorek, M Mar García González, Silvia Azzarello-Burri, Christiane Spaich, May-Britt Harmsen, Anita Rauch, Martin Zenker, Dietmar Müller, Peter Meinecke, Eva Seemanova, Eva Rossier, Bernhard Steiner, Gabriele Gillessen-Kaesbach |
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| Přispěvatelé: | University of Zurich, Kutsche, K |
| Rok vydání: | 2009 |
| Předmět: |
Male
2716 Genetics (clinical) 10039 Institute of Medical Genetics DNA Mutational Analysis 610 Medicine & health Biology medicine.disease_cause Polymorphism Single Nucleotide Microphthalmia Article X-inactivation 1311 Genetics Genes X-Linked Genetics medicine Humans Microphthalmos Genetics (clinical) Chromosomes Human X Mutation Anophthalmia Models Genetic Membrane Proteins Dysostosis HCCS medicine.disease Focal dermal hypoplasia PORCN Focal Dermal Hypoplasia Alternative Splicing Phenotype Child Preschool 570 Life sciences biology Female Acyltransferases |
| Zdroj: | European Journal of Human Genetics. 17:1207-1215 |
| ISSN: | 1476-5438 1018-4813 |
| DOI: | 10.1038/ejhg.2009.40 |
| Popis: | Focal dermal hypoplasia (FDH) is an X-linked developmental disorder with male lethality characterized by patchy dermal hypoplasia, skeletal and dental malformations, and microphthalmia or anophthalmia. Recently, heterozygous loss-of-function mutations in the PORCN gene have been described to cause FDH. FDH shows some clinical overlap with the microphthalmia with linear skin defects (MLS) syndrome, another X-linked male lethal condition, associated with mutations of HCCS in the majority of cases. We performed DNA sequencing of PORCN in 13 female patients with the clinical diagnosis of FDH as well as four female patients with MLS syndrome and no mutation in HCCS. We identified PORCN mutations in all female patients with FDH. Eleven patients seem to have constitutional PORCN alterations in the heterozygous state and two individuals are mosaic for the heterozygous sequence change in PORCN. No PORCN mutation was identified in the MLS-affected patients, providing further evidence that FDH and MLS do not overlap genetically. X chromosome inactivation (XCI) analysis revealed a random or slightly skewed XCI pattern in leukocytes of individuals with intragenic PORCN mutation suggesting that defective PORCN does not lead to selective growth disadvantage, at least in leukocytes. We conclude that the PORCN mutation detection rate is high in individuals with a clear-cut FDH phenotype and somatic mosaicism can be present in a significant proportion of patients with mild or classic FDH. |
| Databáze: | OpenAIRE |
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