Conditions / Genetic

retinitis pigmentosa 59

info · Genetic · ICD-10: H35.5

A retinitis pigmentosa that has_material_basis_in mutation in the DHDDS gene on chromosome 1p36.11.

Signs and symptoms

  • Constriction of peripheral visual field
  • Nyctalopia
  • Reduced visual acuity
  • Rod-cone dystrophy
  • Axial hypotonia
  • Micropenis
  • Feeding difficulties
  • Seizure
  • Renal insufficiency
  • Hepatomegaly

Also known as: RP59