Bietti crystalline retinopathy (Q84185): Difference between revisions

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Latest revision as of 09:32, 15 August 2026

Bietti crystalline retinopathy is a rare progressive autosomal recessive tapetoretinal degeneration disease, occurring in the third decade of life, characterised by small sparkling crystalline deposits in the posterior retina and corneal limbus in addition to sclerosis of the choroidal vessels and manifesting as nightblindness, decreased vision, paracentral scotoma, and, in the end stages of the disease, legal blindness.

Language	Label	Description	Also known as
default for all languages	ID_1922709888
English	Bietti crystalline retinopathy	Bietti crystalline retinopathy is a rare progressive autosomal recessive tapetoretinal degeneration disease, occurring in the third decade of life, characterised by small sparkling crystalline deposits in the posterior retina and corneal limbus in addition to sclerosis of the choroidal vessels and manifesting as nightblindness, decreased vision, paracentral scotoma, and, in the end stages of the disease, legal blindness.