Coats disease

Coats disease (CD) is an idiopathic disorder characterized by retinal telangiectasia with deposition of intraretinal or subretinal exudates, potentially leading to retinal detachment and unilateral blindness. CD is classically an isolated and unilateral condition affecting otherwise healthy young children.

Exudative retinopathy



Total: 3

                       


(per page)
PMID (PMCID)
28424147
(5949049)
 MALE
Treatment of Leukoencephalopathy With Calcifications and Cysts With Bevacizumab.
Fay AJ, King AA, Shimony JS, Crow YJ, Brunstrom-Hernandez JE.
Pediatr Neurol. 2017;71:56-59.
Coats disease without extraocular involvement, a genetically distinct disorder from Coats plus, is characterized by retinal telangiectasias and exudative retinopathy, accompanied by neovascularization.
24635161
 MALE
Retinoschisis in the setting of Coats' disease.
Yannuzzi NA, Tzu JH, Hess DJ, Berrocal AM.
Ophthalmic Surg Lasers Imaging Retina. 2014;45(2):172-4.
This is a report of a 5-year-old boy who presented with an exudative retinopathy consistent with Coats' disease.
3039415
 MALE
Coats' disease in a renal transplant recipient.
Berger M, Lieberman KV, Schoeneman MJ, Schuman JS, Friedman AH.
Nephrol Dial Transplant. 1987;2(2):120-3.
We report the first case, to our knowledge, of Coats' disease, an idiopathic exudative retinopathy, in a renal transplant recipient.