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Aniridia is seen in approximately 1.8/100 000 live births. The incidence ranges from 1:40 000 to 1:100.000. No docHub racial or gender predilection has been described.
Congenital aniridia is a rare disease that affects both eyes. It is autosomal dominant in the majority. Most of the other cases of congenital aniridia are sporadic. Sporadic aniridia may correlate with WAGR syndrome (Wilm tumor, aniridia, genitourinary anomalies, and mental retardation).
Isolated aniridia is the partial or complete absence of the iris from birth. Some people with this type of aniridia may be unaware of any eye problems because pupils appear normal and usually only one eye is mildly affected. In more severe cases, isolated aniridia can cause vision problems later in life.
In general, people with aniridia lack detail vision and have better vision at close range. What can someone with aniridia see? The range of vision is different for each individual with aniridia, and there is not one specific description to explain what someone with aniridia can see.
Aniridia occurs in 1 in 50,000 to 100,000 newborns worldwide.
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Generally, individuals with aniridia have a visual acuity measurement between 20/80 and 20/200. Some are legally blind, while others have vision good enough to drive a car. Most read without using Braille, especially in todays technically advanced environment of e-Readers and smart devices.
How common is aniridia? Aniridia affects around one in every 75,000 babies born each year worldwide. Its more common in children whose biological parents also have aniridia. Around two-thirds of babies born with aniridia have a parent who also has it.

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