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A case of phakomatosis pigmentovascularis association with congenital temporal alopecia / 대한피부과학회지
Article en Ko | WPRIM | ID: wpr-110682
Biblioteca responsable: WPRO
ABSTRACT
Phakomatosis pigmentovascularis is characterized by the coexistence of pigmentary and vascular nevi, which are occasionally associated with systemic organ involvement. We report a 12-year-old male, who showed bilateral nevus of Ota on the forehead, periorbital area, sclera and soft palate, nevus of Ito on the scapular area, mongolian spot on the sacral area and widespread nevus flammeus. He was also associated with congenital temporal alopecia on the lower portion of left temporal region since birth.
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Texto completo: 1 Índice: WPRIM Asunto principal: Paladar Blando / Esclerótica / Nevo de Ota / Mancha Vino de Oporto / Síndromes Neurocutáneos / Parto / Mancha Mongólica / Alopecia / Frente / Nevo Límite: Child / Humans / Male Idioma: Ko Revista: Korean Journal of Dermatology Año: 1991 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Paladar Blando / Esclerótica / Nevo de Ota / Mancha Vino de Oporto / Síndromes Neurocutáneos / Parto / Mancha Mongólica / Alopecia / Frente / Nevo Límite: Child / Humans / Male Idioma: Ko Revista: Korean Journal of Dermatology Año: 1991 Tipo del documento: Article