| Literature DB >> 1302142 |
G De Wilde1, M Hansens, P Govaert.
Abstract
The Walker-Warburg syndrome is characterized by lissencephaly type II, cerebellar and retinal anomalies and congenital muscular dystrophy. A clinical and histopathological study of a case is presented and the differential diagnosis discussed.Entities:
Mesh：
Year: 1992 PMID： 1302142
Source DB: PubMed Journal: Bull Soc Belge Ophtalmol ISSN： 0081-0746