A Case of Rieger's Syndrome Associated with Controlled Glaucoma
Journal of the Korean Ophthalmological Society
;
: 890-895, 1995.
Article
Dans Coréen
| WPRIM
| ID: wpr-226981
ABSTRACT
Rieger's syndrome is a rare autosomal dominant developmental anomaly characterized by ocular and systemic abnomalities. These disorders are typically bilateral and usually diagnosed at birth or in the childhood. The most common ocular defects are hypoplasia of the iris, a prominent Schwalbe's line with iris strands and corectopia. A large number of patients have glaucoma due to devel-opmental defects of the anterior chamber angle structure. The authors experienced a case of Rieger's syndrome which was found in 31-year-old female, who had characteristic ocular and other systemic abnormalities. Associated glaucoma was well controlled by filtering surgery.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Nerf optique
/
Atrophie
/
Peau
/
Pression intracrânienne
/
Atrophie optique
/
Atteintes du nerf optique
/
Glaucome
/
Iris
/
Neurofibromatoses
/
Glioblastome
Limites du sujet:
Adulte
/
Femelle
/
Humains
langue:
Coréen
Texte intégral:
Journal of the Korean Ophthalmological Society
Année:
1995
Type:
Article
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