retinitis pigmentosa 37

A retinitis pigmentosa that has_material_basis_in mutation in the NR2E3 gene on chromosome 15q23.

Signs and symptoms

• Nyctalopia
• Reduced visual acuity
• Rod-cone dystrophy
• Constriction of peripheral visual field
• Tritanomaly
• Pigmentary retinopathy
• Red-green dyschromatopsia
• Undetectable light- and dark-adapted electroretinogram
• Posterior subcapsular cataract
• Photophobia

Also known as: RP37