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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Detalles Bibliográficos
Autores principales: Corte, Liliam Dalla, da Silva, Mariana Vale Scribel, de Oliveira, Carina Flores, Vetoratto, Gerson, Steglich, Raquel Bissacotti, Borges, Josiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875996/
https://www.ncbi.nlm.nih.gov/pubmed/24346921
http://dx.doi.org/10.1590/abd1806-4841.20132135

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875996/
https://www.ncbi.nlm.nih.gov/pubmed/24346921
http://dx.doi.org/10.1590/abd1806-4841.20132135

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