| Literature DB >> 2276038 |
A A Gabreëls-Festen1, E M Joosten, F J Gabreëls, D F Stegeman, A J Vos, H F Busch.
Abstract
Six patients (5 index cases and 1 sib) with a congenital motor and sensory neuropathy are described. The clinical, genetic and electrophysiological features resembled Dejerine-Sottas disease or hereditary motor and sensory neuropathy (HMSN) type III. Sural nerve biopsy of 5 patients revealed segmental demyelination and remyelination with hypertrophic changes, although onion bulbs were not as ubiquitous as in classical HMSN type III. A striking discriminating feature from HMSN type III was an abundance of focal myelin thickenings (tomacula) present in nearly all teased fibres. Possible pathogenic implications are discussed. These cases corroborate the heterogeneity of congenital motor and sensory neuropathies.Entities:
Mesh:
Year: 1990 PMID: 2276038 DOI: 10.1093/brain/113.6.1629
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501