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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Détails bibliographiques
Auteurs principaux: Corte, Liliam Dalla, da Silva, Mariana Vale Scribel, de Oliveira, Carina Flores, Vetoratto, Gerson, Steglich, Raquel Bissacotti, Borges, Josiane
Format: Artigo
Langue:Inglês
Publié: Sociedade Brasileira de Dermatologia 2013
Sujets:
Case Report
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3875996/
https://ncbi.nlm.nih.gov/pubmed/24346921
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20132135
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