Unusual retinal manifestation in a combination of Sturge-Weber and Klipplel-Trenaunay syndrome--a case report.
Indian J Ophthalmol
;
1990 Oct-Dec; 38(4): 195-7
Article
Dans Anglais
| IMSEAR
| ID: sea-70807
ABSTRACT
An unusual retinal manifestation of arteriovenous communications is reported in a case showing a combination of Sturge-Weber and Kippel-Trenaunay syndromes. The arteriovenous communications are thought to be similar to those seen in the limbs in Parkes-Weber syndrome. This retinal finding indicates that the three syndromes are intricately related to each other and may be an incomplete manifestation of a single pathophysiologic entity which may be named neurocutaneous angiomatosis.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Malformations artérioveineuses
/
Artère centrale de la rétine
/
Veine centrale de la rétine
/
Humains
/
Mâle
/
Angiographie fluorescéinique
/
Syndrome de Sturge-Weber
/
Adolescent
/
Syndrome de Klippel-Trénaunay
/
Fond de l'oeil
langue:
Anglais
Texte intégral:
Indian J Ophthalmol
Année:
1990
Type:
Article
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