Conditions / Genetic
retinitis pigmentosa 28
info · Genetic · ICD-10: H35.5
A retinitis pigmentosa that has_material_basis_in mutation in the FAM161A gene on chromosome 2p15.
Signs and symptoms
- Constriction of peripheral visual field
- Spicular pigmentation of the retina
- Nyctalopia
- Rod-cone dystrophy
- Optic disc pallor
Also known as: RP28