Conditions / Genetic

retinitis pigmentosa 2

info · Genetic · ICD-10: H35.5

A retinitis pigmentosa that has_material_basis_in mutation in the RP2 gene on chromosome Xp11.3.

Signs and symptoms

  • Myopia
  • Atrophic fundus lesion
  • High myopia
  • Central scotoma
  • Constriction of peripheral visual field
  • Nyctalopia
  • Pigmentary retinopathy
  • Cataract
  • Rod-cone dystrophy
  • Chorioretinal atrophy

Also known as: RP2