Conditions / Genetic
retinitis pigmentosa 69
info · Genetic · ICD-10: H35.5
A retinitis pigmentosa that has_material_basis_in mutation in the KIZ gene on chromosome 20p11.
Signs and symptoms
- Perifoveal hypoautofluorescence
- Nyctalopia
- Pigmentary retinopathy
- Rod-cone dystrophy
- Constriction of peripheral visual field
- Reduced visual acuity
- Undetectable electroretinogram
Also known as: RP69