MRCS syndrome

MRCS syndrome is a rare, genetic retinal dystrophy disorder characterized by bilateral microcornea, rod-cone dystrophy, cataracts and posterior staphyloma, in the absence of other systemic features. Night blindness is typically the presenting manifestation and nystagmus, strabismus, astigmatism and angle closure glaucoma may be associated findings. Progressive visual acuity deterioration, due to pulverulent-like cataracts, results in poor vision ranging from no light perception to 20/400.

Also known as: microcornea-rod-cone dystrophy-cataract-posterior staphyloma syndrome

25 clinical trials for this condition and its sub-types, 0 tagged with MRCS syndrome itself.