| Literature DB >> 21373256 |
N M Haddad1, D Ente, E Chouery, N Jalkh, C Mehawej, Z Khoueir, V Pingault, A Mégarbané.
Abstract
Waardenburg syndrome (WS) is a genetic disorder characterized primarily by depigmentation of the skin and hair, heterochromia of the irides, sensorineural deafness, and sometimes by dystopia canthorum, and Hirschsprung disease. WS presents a large clinical and genetic heterogeneity. Four different types have been individualized and linked to 5 different genes. We report 2 cases of WS type II and 1 case of WS type IV from Lebanon and Syria. The genetic studies revealed 2 novel mutations in the MITF gene of the WS type II cases and 1 novel homozygous mutation in the EDNRB gene of the WS type IV case. This is the first molecular study of patients from the Arab world. Additional cases will enable a more detailed description of the clinical spectrum of Waardenburg syndrome in this region.Entities:
Year: 2011 PMID: 21373256 PMCID: PMC3042120 DOI: 10.1159/000322891
Source DB: PubMed Journal: Mol Syndromol ISSN: 1661-8769