Monilethrix: a typical case report with microscopic and dermatoscopic findings
An. bras. dermatol
; 90(1): 126-127, Jan-Feb/2015. graf
Article
em En
| LILACS
| ID: lil-735741
Biblioteca responsável:
BR1.1
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.
Palavras-chave
Texto completo:
1
Índice:
LILACS
Assunto principal:
Dermoscopia
/
Monilétrix
Tipo de estudo:
Diagnostic_studies
Limite:
Child
/
Female
/
Humans
Idioma:
En
Revista:
An. bras. dermatol
Assunto da revista:
DERMATOLOGIA
Ano de publicação:
2015
Tipo de documento:
Article