Summary
A pedigree with a new form of hereditary sensory neuropathy is described. Ataxia and scoliosis rather than loss of pain and ulcerating acropathy are the principal clinical features. Analysis of the pedigree suggests a dominant mode of transmission with variable age of onset and perhaps reduced penetrance.
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Robinson, G.C., Jan, J.E. & Miller, J.R. A new variety of hereditary sensory neuropathy. Hum Genet 35, 153–161 (1977). https://doi.org/10.1007/BF00393964
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DOI: https://doi.org/10.1007/BF00393964