Conditions / Genetic

retinitis pigmentosa 45

info · Genetic · ICD-10: H35.5

A retinitis pigmentosa that has_material_basis_in mutation in the CNGB1 gene on chromosome 16q13.

Signs and symptoms

  • Spicular pigmentation of the retina
  • Nyctalopia
  • Peripheral visual field loss
  • Rod-cone dystrophy
  • Abnormal electroretinogram
  • Macular degeneration

Also known as: RP45