X-linked retinal dysplasia
A rare genetic eye disease characterized by abnormal proliferation of retinal tissue resulting in the formation of retinal folds thereby causing gliosis and clinically variable degrees of visual impairment. No clinical findings other than those associated with the eyes have been demonstrated.
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
X-linked retinal dysplasia?
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Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
For a list of clinical trials in this disease area, please click here.