Vohwinkel syndrome, ichthyosiform variant - by Camisa - Case report

Vohwinkel syndrome, ichthyosiform variant - by Camisa - Case report

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 pre...

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Bibliographic Details
Main Authors: Liliam Dalla Corte, Mariana Vale Scribel da Silva, Carina Flores de Oliveira, Gerson Vetoratto, Raquel Bissacotti Steglich, Josiane Borges
Format: Article
Language:English
Published: Sociedade Brasileira de Dermatologia 2013-12-01
Series:Anais Brasileiros de Dermatologia
Subjects:
Dyskeratosis congenita
Finger injuries
Hand dermatoses
Ichthyosis
Keratoderma, palmoplantar
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000800206&tlng=en

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http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000800206&tlng=en

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