| Literature DB >> 2377348 |
K J Murphy1, R PeBenito, R L Storm, C Ferretti, D P Liu.
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.Entities:
Mesh:
Year: 1990 PMID: 2377348 DOI: 10.3109/13816819009012954
Source DB: PubMed Journal: Ophthalmic Paediatr Genet ISSN: 0167-6784