Conditions / Genetic

retinitis pigmentosa 38

info · Genetic · ICD-10: H35.5

A retinitis pigmentosa that has_material_basis_in mutation in the MERTK gene on chromosome 2q13.

Signs and symptoms

  • Constriction of peripheral visual field
  • Nyctalopia
  • Progressive visual loss
  • Rod-cone dystrophy
  • Peripheral retinal atrophy
  • Macular atrophy
  • Optic disc pallor

Also known as: RP38