Coats' disease results in a gradual loss of vision.

One early warning sign of Coats' disease is yellow-eye in flash photography.

These angiomatous lesions were consistent with a variant of Coats' disease.

Glaucoma, atrophy, and cataracts can also develop secondary to Coats' disease.

Although Coats' disease tends to progress to visual loss, it may stop progressing on its own, either temporarily or permanently.

Coats' disease is named after George Coats.

Coats' disease itself is painless.

In moderate to severe Coats' disease, massive retinal detachment and hemorrhage from the abnormal vessels may be seen.

A white eye reflection is not always a positive indication of retinoblastoma and can be caused by light being reflected badly or by other conditions such as Coats' disease.

On funduscopic eye examination, the retinal vessels in early Coats' disease appear tortuous and dilated, mainly confined to the peripheral and temporal portions of retina.

Coats' disease is an exudative detachment of the retina, associated with vascular abnormalities including telangiectatic vessels, microaneurysms, areas of non-perfusion, and saccular venous dilatations.

On ultrasound, Coats' disease appears as a hyperechoic mass in the posterior vitreous without posterior acoustic shadowing; vitreous and subretinal hemorrhage may often be observed.

Some have described IJRT as a variant of Coats' disease, although this is a more accurate depiction of the Type 1 form than the Type 2 form.

Coats' disease is thought to result from breakdown of the blood-retinal barrier in the endothelial cell, resulting in leakage of blood products containing cholesterol crystals and lipid-laden macrophages into the retina and subretinal space.

Coats' disease, (also known as exudative retinitis or retinal telangiectasis, sometimes spelled Coates' disease), is a very rare congenital, nonhereditary eye disorder, causing full or partial blindness, characterized by abnormal development of blood vessels behind the retina.

Coats' disease, (also known as exudative retinitis or retinal telangiectasis, sometimes spelled Coates' disease), is a very rare congenital, nonhereditary eye disorder, causing full or partial blindness, characterized by abnormal development of blood vessels behind the retina.

Coats Syndrome Retinal Telangiectasis None Coats disease is a rare disorder characterized by abnormal development of the blood vessels of the nerve-rich membrane lining the eyes (retina).

Coats' disease, (also known as exudative retinitis or retinal telangiectasis, sometimes spelled Coates' disease), is a very rare congenital, nonhereditary eye disorder, causing full or partial blindness, characterized by abnormal development of blood vessels behind the retina.