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Walker-Warburg syndrome. Case report and literature review.

作者信息

Murphy K J, PeBenito R, Storm R L, Ferretti C, Liu D P

机构信息

Stanley S. Lamm Institute for Child Neurology and Developmental Medicine, Department of Pediatrics, Long Island College Hospital, Brooklyn, NY 11201.

出版信息

Ophthalmic Paediatr Genet. 1990 Jun;11(2):103-8. doi: 10.3109/13816819009012954.

Abstract

The Walker-Warburg syndrome (WWS) is a fatal dysmorphic disorder of unknown etiology, but strongly suggests an autosomal recessive mode of inheritance. It is characterized by severe congenital oculo-cerebral malformations (lissencephaly, congenital hydrocephalus, and ocular lesions). The authors report a case of WWS that occurred in a consanguineous union, with a review of the literature. Possible pathogenesis, and disorders sharing the features of WWS are discussed. Families-at-risk for WWS should be identified for prenatal diagnosis and for genetic counselling.

摘要

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