Autosomal dominant vitreoretinochoroidopathy
A rare genetic vitreous-retinal disease characterized by ocular developmental anomalies such as microcornea a shallow anterior chamber glaucoma and cataract. Abnormal chorioretinal pigmentation is present usually lying between the vortex veins and the ora serrata for 360 degrees.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.
Newly diagnosed with
Autosomal dominant vitreoretinochoroidopathy?
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Syndromes Without A Name (SWAN) Australia
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