retinitis pigmentosa 10

A retinitis pigmentosa that has_material_basis_in mutation in the IMPDH1 gene on chromosome 7q32.

Signs and symptoms

• Constriction of peripheral visual field
• Spicular pigmentation of the retina
• Nyctalopia
• Bull's eye maculopathy
• Reduced visual acuity
• Optic disc pallor
• Attenuation of retinal blood vessels
• Macular geographic atrophy
• Rod-cone dystrophy
• Undetectable light- and dark-adapted electroretinogram

Also known as: RP10