retinitis pigmentosa 11

A retinitis pigmentosa that has_material_basis_in mutation in the PRPF31 gene on chromosome 19q13.

Signs and symptoms

• Nyctalopia
• Perifoveal ring of hyperautofluorescence
• Macular edema
• Constriction of peripheral visual field
• Spicular pigmentation of the retina
• Blindness
• Reduced visual acuity
• Rod-cone dystrophy
• Optic disc pallor
• Macular degeneration

Also known as: RP11