Article
Olmsted syndrome: clinical, molecular and therapeutic aspects.
Orphanet journal of rare diseases - 17 Mar 2015
Duchatelet Sabine, Hovnanian Alain
Abstract excerpt
Olmsted syndrome (OS) is a rare genodermatosis classically characterized by the combination of bilateral mutilating transgredient palmoplantar keratoderma (PPK) and periorificial keratotic plaques, but which shows considerable clinical heterogeneity. The disease starts usually at birth or in early childhood. About 73 cases have been reported worldwide. OS is observed in both sexes, although male cases are more...
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