Acorea, microphthalmia and cataract syndrome
| Acorea, microphthalmia and cataract syndrome | |
|---|---|
| Specialty | Ophthalmology |
Acorea, microphthalmia and cataract syndrome is a rare genetically inherited condition.[1]
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]
![[icon]](/wiki/File:Wiki_letter_w_cropped.svg){kind=small} | This section is empty. You can help by adding to it. (December 2017) |
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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