| Literature DB >> 6316205 |
M L Grunnet, A W Zimmerman, R A Lewis.
Abstract
Cockayne's syndrome is a multisystem disease that begins in infancy and is inherited as an autosomal recessive. We studied a 4-year-old girl with nystagmus, ataxia, motor weakness, peripheral neuropathy, deficient growth, and developmental delay. Nerve biopsy revealed segmental demyelination and granular lysosomal inclusions on ultrastructural examination.Entities:
Mesh:
Year: 1983 PMID: 6316205 DOI: 10.1212/wnl.33.12.1606
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910