| Literature DB >> 206509 |
Abstract
Two brothers with a new type of hereditary sensory neuropathy are described. The main clinical feature is late onset sensory ataxia without ulcerating acropathy or other autonomic abnormality. The older patient also has oculomotor dysfunction and extensor plantar responses.Entities:
Mesh:
Year: 1978 PMID: 206509 DOI: 10.1007/bf00291634
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132