Por favor, use este identificador para citar o enlazar este ítem:
https://www.arca.fiocruz.br/handle/icict/9732
Tipo
ArtículoDerechos de autor
Acceso abierto
Colecciones
- IFF - Artigos de Periódicos [1284]
Metadatos
Mostrar el registro completo del ítem
MONILETHRIX: A TYPICAL CASE REPORT WITH MICROSCOPIC AND DERMATOSCOPIC FINDINGS
Afiliación
Fundação Oswaldo Cruz. Instituto Fernandes Figueira. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Fernandes Figueira. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Fernandes Figueira. Rio de Janeiro, RJ, Brasil.
Resumen en ingles
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.
Compartir