Autosomal recessive pericentral pigmentary retinopathy

MONDO:0009987

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.

Also known as: retinitis pigmentosa, pericentral, retinopathy, pericentral pigmentary, autosomal recessive

33 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by