Aniridia is a rare congenital genetic disease, characterized by the absence of the iris. It's accompanied by photophobia, nystagmus, a strong decrease in visual acuity, with possible corneal degeneration, cataracts, glaucoma and other eye problems. In addition, aniridia may also be accompanied by pathologies of other organs and systems (nervous system, urinary system, endocrine system, digestion and other).
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