| 词条 | Acorea, microphthalmia and cataract syndrome |
| 释义 |
| name = | synonym = | image = | image_size = | alt = | caption = | pronounce = | specialty = ophthalmology | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Acorea, microphthalmia and cataract syndrome is a rare genetically inherited condition.[1] Clinical featuresAcorea 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. GeneticsThe cause of this condition is not presently known. It appears to be inherited in an autosomal dominant fashion. Diagnosis{{Empty section|date=December 2017}}Treatment{{Empty section|date=December 2017}}References1. ^Kondo H, Tahira T, Yamamoto K, Tawara A (2013) Familial acorea, microphthalmia and cataract syndrome. Br J Ophthalmol {{Congenital malformations and deformations of eye, ear, face and neck}}{{Medicine}} 4 : Genetic disorders by system|Congenital disorders of eyes|Syndromes affecting the eyes|Rare syndromes |
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