Conditions / Genetic
retinitis pigmentosa 68
info · Genetic · ICD-10: H35.5
A retinitis pigmentosa that has_material_basis_in mutation in the SLC7A14 gene on chromosome 3q26.
Signs and symptoms
- Spicular pigmentation of the retina
- Nyctalopia
- Visual field defect
- Reduced visual acuity
- Rod-cone dystrophy
- Retinal atrophy
Also known as: RP68