Autosomal dominant rhegmatogenous retinal detachment
A rare hereditary non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present.
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 rhegmatogenous retinal detachment?
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Advocacy Organizations
Syndromes Without A Name (SWAN) Australia
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Clinical Trials
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