Conditions / Genetic
retinitis pigmentosa 60
info · Genetic · ICD-10: H35.5
A retinitis pigmentosa that has_material_basis_in mutation in the PRPF6 gene on chromosome 20q13.33.
Signs and symptoms
- Constriction of peripheral visual field
- Spicular pigmentation of the retina
- Nyctalopia
- Reduced visual acuity
- Visual impairment
- Peripheral visual field loss
- Rod-cone dystrophy
- Retinal pigment epithelial atrophy
- Attenuation of retinal blood vessels
- Posterior subcapsular cataract
Also known as: RP60