Vohwinkel syndrome, ichthyosiform variant - by Camisa - Case report

• Main Authors: Liliam Dalla Corte (Author), Mariana Vale Scribel da Silva (Author), Carina Flores de Oliveira (Author), Gerson Vetoratto (Author), Raquel Bissacotti Steglich (Author), Josiane Borges (Author)
• Format: Book
• Published: Sociedade Brasileira de Dermatologia, 2013-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...