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Аутосомно-домінантний кератит

ORPHA:2334· ICD-10 H16.8· Autosomal dominant keratitis

Визначення(English summary)

A rare genetic inflammatory corneal disorder characterized by anterior stromal corneal opacification and vascularization of the peripheral cornea with potential central progression and subsequent reduction in visual acuity. Variable features include abnormalities of the iris, such as stromal defects and ectropion uveae, as well as foveal hypoplasia.

Поширеність
Unknown
Успадкування
Autosomal dominant
Вік початку
Childhood