Article
Vohwinkel syndrome, ichthyosiform variant--by Camisa--case report.
Anais brasileiros de dermatologia - 1 Jan 2000
Corte Liliam Dalla, Silva Mariana Vale Scribel da, Oliveira Carina Flores de, Vetoratto Gerson, Steglich Raquel Bissacotti, Borges Josiane
Abstract excerpt
Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar keratosis, which manifests in infants and becomes more evident in adulthood. Its mode of inheritance is autosomal dominant with mutation in loricrin and Connexin 26 genes. Patients with this mutation present hyperkeratosis of the palms and soles, constricting bands of the digits, usually on the fifth, and...
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