Conditions / Genetic

retinitis pigmentosa 60

info · Genetic · ICD-10: H35.5

A retinitis pigmentosa that has_material_basis_in mutation in the PRPF6 gene on chromosome 20q13.33.

Signs and symptoms

  • Constriction of peripheral visual field
  • Spicular pigmentation of the retina
  • Nyctalopia
  • Reduced visual acuity
  • Visual impairment
  • Peripheral visual field loss
  • Rod-cone dystrophy
  • Retinal pigment epithelial atrophy
  • Attenuation of retinal blood vessels
  • Posterior subcapsular cataract

Also known as: RP60