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Am J Med Genet. 1994 Jan 15;49(2):198-201.

Walker-Warburg syndrome: report of three affected sibs.

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  • 1Department of Pediatrics, Medical University of South Carolina, Charleston 29425.

Abstract

Walker-Warburg syndrome (WWS) is a lethal, autosomal recessive disorder characterized by Type II lissencephaly, retinal malformation, cerebellar malformation, and congenital muscular dystrophy. We report on 3 sibs with WWS born to a consanguineous couple. The fetal hydrocephalus associated with this syndrome, while not consistent or necessary for diagnosis, is the key manifestation for its prenatal detection. These sibs illustrate the importance of a careful search for associated malformation(s) in a fetus or newborn infant with hydrocephalus and the potential pitfalls of accurate genetic risk estimation in families of such propositi.

PMID:
8116667
[PubMed - indexed for MEDLINE]
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