retinitis pigmentosa 26

A retinitis pigmentosa that has_material_basis_in mutation in the CERKL gene on chromosome 2q31.

Signs and symptoms

• Constriction of peripheral visual field
• Visual impairment
• Optic disc pallor
• Undetectable light- and dark-adapted electroretinogram
• Rod-cone dystrophy
• Attenuation of retinal blood vessels

Also known as: RP26