1.
An. bras. dermatol
; 90(1): 126-127, Jan-Feb/2015. graf
Artigo
em Inglês
| LILACS
| ID: lil-735741
RESUMO
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.