Monilethrix: a typical case report with microscopic and dermatoscopic findings

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...

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Bibliographic Details
Published inAnais brasileiros de dermatología Vol. 90; no. 1; pp. 126 - 127
Main Authors Oliveira, Elisa Fontenelle de, Araripe, Ana Luiza Cotta de Alencar
Format Journal Article
LanguageEnglish
Published Brazil Sociedade Brasileira de Dermatologia 01.01.2015
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