Harvard Catalyst Profiles

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Keratoderma, Palmoplantar, Epidermolytic

"Keratoderma, Palmoplantar, Epidermolytic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

An autosomal dominant hereditary skin disease characterized by epidermolytic hyperkeratosis that is strictly confined to the palms and soles. It has been associated with mutations in the gene that codes for KERATIN-9.

This graph shows the total number of publications written about "Keratoderma, Palmoplantar, Epidermolytic" by people in Harvard Catalyst Profiles by year, and whether "Keratoderma, Palmoplantar, Epidermolytic" was a major or minor topic of these publication.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.