| Literature DB >> 9120454 |
R M Chalmers1, P Riordan-Eva, N W Wood.
Abstract
Three siblings are reported with childhood onset hereditary motor and sensory neuropathy (HMSN) and adult onset optic atrophy. Electrophysiological studies showed an axonal neuropathy and dysfunction of the retinal ganglion cells or optic nerve. The presumed mode of inheritance is autosomal recessive. This is the second family in which autosomal recessive inheritance of HMSN and optic atrophy (HMSN type VI) has been described, and the first in which electrophysiological studies have been reported.Entities:
Mesh:
Year: 1997 PMID: 9120454 PMCID: PMC1074097 DOI: 10.1136/jnnp.62.4.385
Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN: 0022-3050 Impact factor: 10.154