Autosomal dominant neovascular inflammatory vitreoretinopathy

Orpha code: 329211OMIM code: 193235

Definition

A rare, genetic, vitreoretinal degeneration characterized by a slowly progressive vitreoretinopathy with onset during the second or third decade of life. The disease initially presents as autoimmune uveitis with reduction in the b-wave on electroretinography, and progresses with development of photoreceptor degeneration, vitreous hemorrhage, cystoid macular edema, retinal neovascularization, intraocular fibrosis, secondary glaucoma, and retinal detachment leading to phthisis and complete blindness.

Disease data
Classification

Disease

Synonyms
ADNIV
ADNIV
ORPHA code
329211
OMIM code
193235
ICD10 code
H35.2
ICD11 code
-

No additional description.

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