Congenital microcoria

Congenital microcoria is a rare autosomal dominant ophthalmological disease caused by maldevelopment of the dilator muscle of the pupil that is characterized by small pupils (<2 mm in diameter) from birth, peripheral iris hypopigmentation and transillumination defects leading to errors of refraction (myopia, astigmatism) and sometimes juvenile open angle glaucoma.

Also known as: congenital miosis, Mcor, chromosome 13Q32 deletion syndrome, microcoria, congenital, miosis, congenital, pinhole pupils

2 clinical trials for this condition and its sub-types, 1 tagged with Congenital microcoria itself.