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Congenital microcoria

ORPHA:566· ICD-10 Q13.8

Definition

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.

Prevalence
Unknown
Inheritance
Autosomal dominant
Age of onset
Infancy, Neonatal