A Case of Sturge-Weber Syndrome
Journal of the Korean Ophthalmological Society
; : 459-464, 1989.
Article
en Ko
| WPRIM
| ID: wpr-223014
Biblioteca responsable:
WPRO
ABSTRACT
Sturge-Weber syndrome is a congenital disorder characterized by facial nevus flammeus along the distribution of the trigeminal nerve, ipsilatal leptomeningioma, buphthalmos, and choroidal angioma. The Authors experienced a case of Sturge-Weber syndrome in 9 year old female patient and glaucoma was controlled by trabecuectomy without any complications.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Nervio Trigémino
/
Síndrome de Sturge-Weber
/
Glaucoma
/
Hidroftalmía
/
Coroides
/
Mancha Vino de Oporto
/
Hemangioma
/
Enfermedades y Anomalías Neonatales Congénitas y Hereditarias
Límite:
Child
/
Female
/
Humans
Idioma:
Ko
Revista:
Journal of the Korean Ophthalmological Society
Año:
1989
Tipo del documento:
Article