retinitis pigmentosa 90

info · Genetic

A retinitis pigmentosa characterized by onset in the first decade of life of night blindness that has_material_basis_in homozygous or compound heterozygous mutation in the IDH3A gene on chromosome 15q25.1.

Signs and symptoms

Nyctalopia
Constriction of peripheral visual field
Attenuation of retinal blood vessels
Reduced visual acuity
Retinal pigment epithelial atrophy
Spicular pigmentation of the retina
Strabismus
Hyperautofluorescent retinal lesion
Cystoid macular edema

Also known as: RP90