Monilethrix: a typical case report with microscopic and dermatoscopic findings

Anais Brasileiros de Dermatologia

Elisa Fontenelle De Oliveira¹  Ana Luiza Cotta De Alencar Araripe¹ 

关键词: Alopecia;    Dermoscopy;    Hypotrichosis;   

DOI  :  10.1590/abd1806-4841.20153357

来源: SciELO

【 摘 要 】

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 topical minoxidil was conducted.

【 授权许可】

CC BY-NC   
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