Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 8708653.
- Also identified by PMC identifier 1073804.
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Abstract
The association between hereditary motor and sensory neuropathy (HMSN) and optic atrophy has been termed HMSN type VI. The autosomal dominant inheritance of this syndrome is reported. Three generations were affected with optic atrophy, which differed in some respects from classic dominant optic atrophy, and an asymptomatic, mainly sensory, neuropathy.
Medical subject headings
- Hereditary Sensory and Motor Neuropathy
- Optic Atrophy