Monilethrix: a typical case report with microscopic and dermatoscopic findings

• Hoofdauteurs: Elisa Fontenelle de Oliveira (Auteur), Ana Luiza Cotta de Alencar Araripe (Auteur)
• Formaat: Boek
• Gepubliceerd in: Sociedade Brasileira de Dermatologia, 2015-02-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

Monilethrix is a rare hereditary condition generally considered to be an autosomal dominant disorder with variable penetrance. A case of a 6-year-old girl without a familial background for this disease is reported. The diagnosis was made by optic microscopy and dermoscopy. A therapeutic trial with t...