Microcoria (Q95311): Difference between revisions

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Latest revision as of 11:03, 16 August 2026

Congenital microcoria is an uncommon bilateral ophthalmological disease marked by partial or complete absence of the dilator muscle of the pupil. At birth, infants have small pupils (< 2 mm) and a far away gaze. The disorder can cause malformations of the anterior part of the eye, leading to errors of refraction (myopia, astigmatism) and sometimes severe juvenile glaucoma. The iridocorneal angle may also be modified and the irides transilluminable. The disease is transmitted as an autosomal dominant trait.

Language	Label	Description	Also known as
default for all languages	ID_290409436
English	Microcoria	Congenital microcoria is an uncommon bilateral ophthalmological disease marked by partial or complete absence of the dilator muscle of the pupil. At birth, infants have small pupils (< 2 mm) and a far away gaze. The disorder can cause malformations of the anterior part of the eye, leading to errors of refraction (myopia, astigmatism) and sometimes severe juvenile glaucoma. The iridocorneal angle may also be modified and the irides transilluminable. The disease is transmitted as an autosomal dominant trait.