A Case of Sturge-Weber Syndrome
Journal of the Korean Ophthalmological Society
;
: 459-464, 1989.
Article
in Korean
| WPRIM
| ID: wpr-223014
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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Trigeminal Nerve
/
Sturge-Weber Syndrome
/
Glaucoma
/
Hydrophthalmos
/
Choroid
/
Port-Wine Stain
/
Hemangioma
/
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Limits:
Child
/
Female
/
Humans
Language:
Korean
Journal:
Journal of the Korean Ophthalmological Society
Year:
1989
Type:
Article
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