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Article

Familial bulbospinal neuronopathy with optic atrophy: a distinct entity.

Journal of neurology, neurosurgery, and psychiatry - 1 Aug 1996

Paradiso G, Micheli F, Taratuto A L, Parera I C

Abstract excerpt

A 61 year old woman and her 58 year old brother presented with the clinical picture of late onset progressive bulbar and spinal muscular atrophy with family history of involvement in successive generations. The sister also had optic neuropathy and the brother developed diabetes mellitus and sex hormone abnormalities. Neurophysiological and histopathological studies showed a pattern of motor and sensory...

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Share to Electromyography
Share to Hereditary Sensory and Motor Neuropathy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Optic Atrophies, Hereditary

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Source

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Identifiers

PMID: 8708690
DOI: 10.1136/jnnp.61.2.196
PMCID: PMC1073996

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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