Cone rod dystrophy

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A rare genetic isolated inherited retinal disorder characterized by primary cone degeneration with significant secondary rod involvement with a variable fundus appearance. Typical presentation includes decreased visual acuity central scotoma photophobia color vision alteration followed by night blindness and loss of peripheral visual field.

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 Data version June 2024

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Cone rod dystrophy?

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