| Literature DB >> 24734328 |
Elzbieta Gawrych, Agnieszka Bińczak-Kuleta, Joanna Janiszewska-Olszowska, Andrzej Ciechanowicz.
Abstract
Ectrodactyly-ectodermal dysplasia-cleft syndrome (EEC) results from a simultaneous developmental abnor-caused by mutations of the tp63 gene. Five mutations: 204, 227, 279, 280, and 304 account for most cases of this syndrome. A case with R304W mutation, characterized by the presence of all major (ectrodactyly, ectodermal dysplasia, cleft lip and palate) and two minor (lacrimal duct obstruction, developmental delay) clinical symptoms of the syndrome is presented. This severe case improves the existing knowledge concerning the genotype-phenotype correlations in EEC syndrome.Entities:
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Year: 2013 PMID: 24734328
Source DB: PubMed Journal: Ann Acad Med Stetin ISSN: 1427-440X