Conditions / Genetic
retinitis pigmentosa 20
info · Genetic · ICD-10: H35.5
A retinitis pigmentosa that has_material_basis_in mutation in the RPE65 gene on chromosome 1p31.
Signs and symptoms
- Nyctalopia
- Nystagmus
- Severely reduced visual acuity
- Visual impairment
- Rod-cone dystrophy
- Attenuation of retinal blood vessels
Also known as: RP20