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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Published in | Anais brasileiros de dermatología Vol. 90; no. 1; pp. 126 - 127 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Brazil
Sociedade Brasileira de Dermatologia
01.01.2015
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Subjects | |
Online Access | Get full text |
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