Autosomal dominant vitreoretinochoroidopathy
Synonyms: ADVIRC
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.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Autosomal dominant vitreoretinochoroidopathy?
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Advocacy Organizations
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
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