Conditions / Genetic
retinitis pigmentosa 33
info · Genetic · ICD-10: H35.5
A retinitis pigmentosa that has_material_basis_in mutation in the SNRNP200 gene on chromosome 2q11.
Signs and symptoms
- Spicular pigmentation of the retina
- Nyctalopia
- Visual impairment
- Optic disc pallor
- Rod-cone dystrophy
- Attenuation of retinal blood vessels
- Retinal pigment epithelial atrophy
Also known as: RP33