Expanding the Phenotypic Spectrum of Olmsted Syndrome

Abstract excerpt

TO THE EDITOR Palmoplantar keratodermas (PPKs) are a group of genetically heterogeneous genodermatoses. Recently mutations in TRPV3 were identified as a cause of the rare form of PPK, Olmsted syndrome (OS; OMIM 614594; Lai-Cheong et al., 2012Lai-Cheong J.E. Sethuraman G. Ramam M. et al.Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome.Br J...

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