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Congenital Sensory NeuropathyReport of an Atypical Case
John R. Person, MD;
Roy S. Rogers III, MD;
K. Hable Rhodes, MD
Arch Dermatol. 1977;113(7):954-957.
Abstract
An otherwise normal 11-year-old boy had greatly reduced acral pain and temperature sensation with associated trophic damage. The disorder was present at birth, and there was no family history of similar problems. The patient also exhibited complete anhidrosis. The case may be an "overlap" between what has been termed as hereditary sensory neuropathy (HSN) type 2 and type 4.
(Arch Dermatol 113:954-957, 1977)
Author Affiliations
From the Mayo Clinic and Mayo Foundation, Rochester, Minn.
Footnotes
Accepted for publication May 3, 1976.
Reprint requests to c/o Section of Publications, Mayo Clinic, 200 First Street SW, Rochester, MN 55901 (Dr Person).
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