retinitis pigmentosa 36

A retinitis pigmentosa that has_material_basis_in mutation in the PRCD gene on chromosome 17q25.

Signs and symptoms

• Undetectable electroretinogram
• Spicular pigmentation of the retina
• Macular degeneration
• Rod-cone dystrophy
• Optic disc pallor
• Attenuation of retinal blood vessels

Also known as: RP36