| Literature DB >> 3673511 |
J M Vallat1, R Gil, M J Leboutet, J Hugon, D Moulies.
Abstract
Two young patients were referred recently to the authors for investigation of a peroneal atrophy syndrome. Since the first symptoms were observed in infancy, a congenital hypomyelination neuropathy was suspected, and superficial peroneal nerve biopsies were taken. Signs of severe and widespread demyelination/remyelination were observed. These features appeared morphologically similar to those observed in the globular or tomaculous neuropathies. The mechanism of the hypermyelination is discussed.Entities:
Mesh:
Year: 1987 PMID: 3673511 DOI: 10.1007/bf00692853
Source DB: PubMed Journal: Acta Neuropathol ISSN: 0001-6322 Impact factor: 17.088