Coats disease


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ex·u·da·tive ret·i·ni·tis

, retinitis exudativa
a chronic abnormality characterized by deposition of cholesterol and cholesterol esters in outer retinal layers and subretinal space. In adults, often preceded by uveitis; in children, often preceded by retinal vascular abnormalities.
Synonym(s): Coats disease

Coats dis·ease

(kōts di-zēz')
A condition with findings that include yellow subretinal exudates and telangiectactic retinal vessels; typically unilateral and often associated with serous retinal detachment.

Coats disease

(kōts)
[George Coats, Brit. ophthalmologist, 1876–1915]
A congenital, unilateral nonhereditary disorder of the retina characterized by aneurysmal dilation of blood vessels with prominent subretinal exudate. This term is used to describe at least six separate retinal disorders.

Coats,

George, English ophthalmologist, 1876-1915.
Coats disease - a chronic abnormality characterized by deposition of cholesterol in outer retinal layers and subretinal space. Synonym(s): exudative retinitis
References in periodicals archive ?
Clinical variations and complications of coats disease in 150 cases: The 2000 Sanford Gifford memorial lecture.
Combined intravitreal bevacizumab and triamcinolone injection in a child with coats disease. J AAPOS 2008;12:309-11.
Demirci, "Clinical variations and complications of Coats disease in 150 cases: the 2000 Sanford Gifford memorial lecture," American Journal of Ophthalmology, vol.
Sigler, "Pearls and pitfalls in diagnosis and management of Coats disease," Retina, vol.
Cater, "Classification and management of Coats disease: the 2000 Proctor Lecture," American Journal of Ophthalmology, vol.
Chen, "The effect of intravitreal bevacizumab in the treatment of coats disease in children," Retina, vol.
Current management of Coats disease. Surv Ophthalmol.
Clinical Characteristics and Treatment Outcomes of Coats Disease in a Saudi Arabian Population.
Disorders less frequently seen in clinical practice - such as uveal coloboma, Coats disease, and rare tumors - are included in its comprehensive coverage.
Coats disease is a rare, idiopathic, predominantly unilateral condition that manifests as severe irregular dilatation, or telangiectasia, of the retinal vasculature.
Although a few cases of Coats disease regress spontaneously, (1) the majority progress over a period of years to massive sub-retinal exudation.
The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease. Br J Ophthalmol.