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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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Detaylı Bibliyografya
Yayımlandı:An Bras Dermatol
Asıl Yazarlar: de Oliveira, Elisa Fontenelle, Araripe, Ana Luiza Cotta de Alencar
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Sociedade Brasileira de Dermatologia 2015
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4323712/
https://ncbi.nlm.nih.gov/pubmed/25672313
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20153357
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