Article
Two familial cases of Olmsted-like syndrome with a G573V mutation of the TRPV3 gene.
Clinical and experimental dermatology - 1 Jul 2016
Zhi Y P, Liu J, Han J W, Huang Y P, Gao Z Q, Yang Y, Wu R N
Abstract excerpt
Olmsted syndrome (OS) is a rare disease, characterized by symmetrical, sharply defined, hyperkeratotic, mutilating plaques on the palms and soles, which are associated with periorificial keratotic plaques. Other clinical manifestations of OS include diffuse alopecia, leucokeratosis of the oral mucosa, onychodystrophy, hyperkeratotic linear streaks, follicular hyperkeratosis and constriction of the digits. A...
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