A rare case of seven siblings with Waardenburg syndrome: a case report

A rare case of seven siblings with Waardenburg syndrome: a case report

Abstract Background Waardenburg syndrome is a group of rare genetic conditions. It is determined by the absence of melanocytes from the eyes, hair, and skin. There are four types of Waardenburg syndrome with specific criteria to diagnosis the different types. The main clinical manifestations are fac...

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Bibliographic Details
Main Authors: Luma Haj Kassem, Mohamed Fares Ahmado, Majd Sheikh Alganameh
Format: Article
Language:English
Published: BMC 2018-07-01
Series:Journal of Medical Case Reports
Subjects:
Waardenburg syndrome
Type 2
Siblings
Hearing loss
Heterochromia
Mutation De novo
Online Access:http://link.springer.com/article/10.1186/s13256-018-1704-1

Internet

http://link.springer.com/article/10.1186/s13256-018-1704-1

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