Sturge-Weber syndrome in association with Klippel-Trenaunay syndrome and phakomatosis pigmentovascularis type IIb.
Indian J Dermatol Venereol Leprol
;
2014 Jan-Feb; 80(1): 51-53
Artículo
en Inglés
| IMSEAR
| ID: sea-154749
ABSTRACT
Phakomatosis pigmentovascularis (PPV) is a rare combination of pigmentary and vascular components with or without systemic involvement. We report here a rare association of Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and PPV type IIb in a 15-year-old boy who had right upper limb monoparesis along with a history of recurrent convulsions.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Fenotipo
/
Trastornos de la Pigmentación
/
Humanos
/
Masculino
/
Síndrome de Sturge-Weber
/
Adolescente
/
Síndrome de Klippel-Trenaunay-Weber
/
Mancha Vino de Oporto
Idioma:
Inglés
Revista:
Indian J Dermatol Venereol Leprol
Año:
2014
Tipo del documento:
Artículo
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