Congenital microcoria

MONDO:0007989

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

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

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