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