Congenital microcoria
MONDO:0007989Congenital 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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Disease
(618)
Hereditary disease
(172)
Eye disorder
(97)
Human disease
(14)
Disorder of orbital region
(3)
Anterior segment dysgenesis
(2)
Disease of genetic or genomic mechanism
(2)
Disorder of visual system
(1)
Disease by body system or component
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Disease by developmental or physiological process
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