학술논문
Monilethrix: a typical case report with microscopic and dermatoscopic findings
Document Type
article
Source
Anais Brasileiros de Dermatologia, Vol 90, Iss 1, Pp 126-127 (2015)
Subject
Language
English
Portuguese
Portuguese
ISSN
0365-0596
1806-4841
1806-4841
Abstract
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.