Conditions / Genetic

autosomal recessive pericentral pigmentary retinopathy

info · Genetic · ICD-10: H35.5

A retinitis pigmentosa that is characterized autosomal recessive inheritance of pigmentary retinal degeneration with onset in the infancy but slower rates of progression than other forms of retinopathy.

Signs and symptoms

  • Astigmatism
  • Strabismus
  • Hypermetropia
  • Pigmentary retinopathy