| Literature DB >> 6737006 |
D Gardner-Medwin, H M Johnston.
Abstract
Twelve girls and 2 boys with severe but not congenital muscular dystrophy were found in a national survey. An autosomal recessive gene is likely to account for most if not all of these cases. The condition differs slightly from X-linked Duchenne muscular dystrophy in showing prominent early toe-walking, a milder course, relatively more weakness of the deltoid muscles, normal intelligence, a normal ECG and a more focal pattern of muscle pathology.Entities:
Mesh:
Substances:
Year: 1984 PMID: 6737006 DOI: 10.1016/0022-510x(84)90058-3
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181