Acorea, microphthalmia and cataract syndrome is a rare genetically inherited condition.[1]
| Acorea, microphthalmia and cataract syndrome | |
|---|---|
| Specialty | Ophthalmology |
Presentation edit
Acorea or fibrous occlusion of the pupil, microphthalmia and cataracts are present in both eyes. Microcornea and iridocorneal dysgenesis also occur. The retina and optic disc are normal.[citation needed]
Genetics edit
The cause of this condition is not presently known. It appears to be inherited in an autosomal dominant fashion.[citation needed]
Diagnosis edit
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Treatment edit
This section is empty. You can help by adding to it. (December 2017) |
References edit
- ^ Kondo H, Tahira T, Yamamoto K, Tawara A (2013) Familial acorea, microphthalmia and cataract syndrome. Br J Ophthalmol
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