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A rare, non-syndromic, hereditary palmoplantar keratoderma characterized by diffuse, yellowish, thick hyperkeratosis of the palms and soles with a sharp ...
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Epidermolytic palmoplantar keratoderma (EPPK; Vörner type) is an autosomal dominant disorder characterized by sharply circumscribed congenital thickening of the ...
Patients with epidermolytic palmoplantar keratoderma (EPPK), an autosomal dominant skin disease, were investigated. Three KRT9 mutations, N160K, R162Q, and ...
Palmoplantar keratodermas are a heterogeneous group of disorders characterized by abnormal thickening of the stratum corneum of the palms and soles.
2) Diffuse epidermolytic palmoplantar keratoderma. (Also known as diffuse EPPK, Vorner disease, PPK cum degenerations granulose) Diffuse epidermolytic PPK is ...
Epidermolytic palmoplantar keratoderma (EPPK) is a rare autosomal dominant skin disorder characterized by diffuse hyperkeratosis on the palms and soles. Whole- ...
EPPK; Epidermolytic palmoplantar keratoderma of Voerner; Epidermolytic palmoplantar keratoderma of Vörner. Prevalence: -. Inheritance: -. Age of onset: Infancy ...
Epidermolytic palmoplantar keratoderma-1 (EPPK1) is an autosomal dominant skin disorder characterized clinically by diffuse, yellow thickening of the skin ...
EPPK from www.nature.com
Patients with epidermolytic palmoplantar keratoderma (EPPK), an autosomal dominant skin disease, were investigated. Three KRT9 mutations, N160K, R162Q, and.