| Literature DB >> 2216592 |
B Simma1, S Felber, H Maurer, I Gassner, S Krassnitzer.
Abstract
We report on a boy with type II lissencephaly and congenital muscular dystrophy. The patient presented with the features of a cerebro-oculo-muscular syndrome (COMS). We describe the clinical presentations and the characteristic sonographic and MR findings.Entities:
Mesh:
Year: 1990 PMID: 2216592 DOI: 10.1007/bf02011390
Source DB: PubMed Journal: Pediatr Radiol ISSN: 0301-0449