diffuse palmoplantar keratoderma
- diffuse palmoplantar keratoderma
- any of several hereditary types of palmoplantar keratoderma; most are autosomal dominant, but a rare type, mal de Meleda, is autosomal recessive. They are usually present in infancy but occasionally do not appear until later. The main characteristic is well-demarcated, usually bilateral and symmetrical, confluent areas of scaling on the palms and soles, sometimes spreading to the backs of the hands and feet. Types are now usually distinguished as either epidermolytic or nonepidermolytic palmoplantar keratoderma depending on whether epidermolysis is present.
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2011.
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Diffuse epidermolytic palmoplantar keratoderma — Classification and external resources OMIM 144200 Diffuse epidermolytic palmoplantar keratoderma (also known as Palmoplantar keratoderma cum degeneratione granulosa Vörner, Vörner s epidermolytic palmoplantar keratoderma , and Vörner keratoderma … Wikipedia
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epidermolytic palmoplantar keratoderma — the most common type of diffuse palmoplantar keratoderma, a genetically heterogeneous, autosomal dominant disorder characterized by epidermolytic hyperkeratosis (q.v.) … Medical dictionary
nonepidermolytic palmoplantar keratoderma — a rare autosomal dominant type of diffuse palmoplantar keratoderma in which there is hyperkeratosis without epidermolysis and characteristic focal oral, genital, and follicular lesions. Called also Unna Thost syndrome … Medical dictionary
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