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Congenital microcoria
rareCongenital 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.
- Identifiers
- MONDO:0007989 OMIM:156600Orphanet:566
- Part of
- Iridogoniodysgenesis
- Also known as
- congenital miosis · pinhole pupils
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