Conditions / Genetic

retinitis pigmentosa 9

info · Genetic · ICD-10: H35.5

A retinitis pigmentosa that has_material_basis_in mutation in the RP9 gene on chromosome 7p14.

Signs and symptoms

  • Constriction of peripheral visual field
  • Spicular pigmentation of the retina
  • Nyctalopia
  • Rod-cone dystrophy
  • Undetectable light- and dark-adapted electroretinogram
  • Macular edema
  • Cataract
  • Macular atrophy

Also known as: RP9