Vohwinkel syndrome

Vohwinkel syndrome: an autosomal dominant, progressive form of palmoplantar keratoderma that begins in childhood, characterized by a stellate pattern of hyperkeratosis on the backs of the hands and feet, linear keratoses on elbows and knees, and annular constrictions of digits like those of ainhum. In some patients it is associated with scarring alopecia and deafness. Called also keratoderma or keratoma hereditarium mutilans.

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Vohwinkel syndrome — Classification and external resources OMIM 124500 DiseasesDB 32216 eMedicine … Wikipedia
Vohwinkel syndrome — Voh·win·kel syndrome (fo vingґkəl) [Karl Hermann Vohwinkel, German dermatologist, 20th century] see under syndrome … Medical dictionary
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Vohwinkel — H.H., 20th century German dermatologist. See V. syndrome … Medical dictionary
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