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Uveal effusion syndrome


Uveal Effusion Syndrome

General: Congenital anomaly of sclera and, in some cases, the vortex vein; inability to transport extravascular protein across abnormal sclera; condition typically affects middle-aged men and causes recurrent, spontaneous serous retinal and ciliochoroidal detachments, often resulting in significant visual impairment.

Ocular: Exudative retinal detachment; sclera abnormally thick; vortex vein obstruction; idiopathic central serous choroidopathy; vitreous cells; ciliochoroidal detachment; nanophthalmos.

Clinical: Viral infection; elevated blood pressure; allergic reaction; minor trauma.

Brubaker RF, Pederson JE. Review-ciliochoroidal detachment. Surv Ophthalmol 1983; 27:281-289.

Gass JD. Uveal effusion syndrome. Retina 1983; 3:159-l63.

Morita H, et al. Recurrence of nanophthalmic uveal effusion. Ophthalmologica 1993; 207:30-36.

Stelmach MZ, et al. Uveal effusion syndrome. Aust N Z J Ophthalmol 1994; 22:139-l43.




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