Conditions / Genetic

retinitis pigmentosa 33

info · Genetic · ICD-10: H35.5

A retinitis pigmentosa that has_material_basis_in mutation in the SNRNP200 gene on chromosome 2q11.

Signs and symptoms

  • Spicular pigmentation of the retina
  • Nyctalopia
  • Visual impairment
  • Optic disc pallor
  • Rod-cone dystrophy
  • Attenuation of retinal blood vessels
  • Retinal pigment epithelial atrophy

Also known as: RP33