Conditions / Genetic
retinitis pigmentosa 18
info · Genetic · ICD-10: H35.5
A retinitis pigmentosa that has_material_basis_in mutation in the PRPF3 gene on chromosome 1q21.
Signs and symptoms
- Nyctalopia
- Focal retinal arteriolar constriction
- Rod-cone dystrophy
- Scotoma
- Progressive visual field defects
Also known as: RP18