Prenatal Diagnosis of Walker–Warburg Syndrome Using Single Nucleotide Polymorphism Array: A Clinical Experience from Three Related Palestinian Families with Congenital Hydrocephalus

Prenatal Diagnosis of Walker–Warburg Syndrome Using Single Nucleotide Polymorphism Array: A Clinical Experience from Three Related Palestinian Families with Congenital Hydrocephalus

Abstract Background Congenital hydrocephalus is a common and often disabling disorder. Various syndromic forms of hydrocephalus have been reported in the Palestinian population including Walker–Warburg syndrome (WWS), Carpenter syndrome, and Meckel syndrome. Aim In this rep...

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Bibliographic Details
Main Authors: Iman S. Abumansour, Eman Al Sulmi, Bernard N. Chodirker, Jennifer C. Hunt
Format: Article
Language:English
Published: Thieme Medical Publishers, Inc. 2015-04-01
Series:American Journal of Perinatology Reports
Subjects:
walker–warburg syndrome
congenital hydrocephalus
prenatal snp array
syndromic hydrocephalus
Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1549298

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