Bietti crystalline retinopathy (Q84185): Difference between revisions

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.