Understanding Aniridia (Aniridia Syndrome)
Aniridia means lack of an iris. It is a rare disorder in which the iris of the eye is partly or completely missing. The iris is the round, colored part of the eye. It controls the size of the pupil and the amount of light that enters the eye.
Aniridia usually affects both eyes. It causes the pupil to be abnormally large. It may also be oddly shaped. The condition can also cause problems with the cornea, lens, retina, and optic nerve. Some of these problems may be present at birth. Others may happen later in life. Problems with other parts of the eye may cause problems that are more severe than the missing iris.
What causes aniridia?
Many cases of aniridia may occur because of a problem with a gene known as PAX6. This gene is passed on from parents to children. The gene helps control eye health and growth. If the PAX6 gene isn’t normal, the eyes may not grow properly. A child of a person with aniridia has a 50% chance of having aniridia. But some children with aniridia don’t have a parent with it. Talk with your child’s healthcare provider if you are interested in genetic testing for other family members.
In most cases, aniridia occurs on its own. But it may be part of a syndrome such as:
WAGR syndrome. This includes a rare kidney cancer called Wilms’ tumor, genital and urinary problems, and mental problems.
Gillespie’s syndrome. This includes mental problems and trouble with balance (ataxia).
Symptoms of aniridia
Symptoms of aniridia can vary. They can include:
Abnormal pupil and iris
Sensitivity to light
Uncontrolled eye movements
Eyes that are uneven or not aligned (strabismus)
Diagnosis of aniridia usually happens early in life. A healthcare provider will ask about your child’s medical history. The provider will also give your child a physical exam. This will include a detailed exam of your child’s eyes. Your child may also have genetic testing to check for the abnormal gene.
March 15, 2019
Aniridia, American Academy of Opthamology, Aniridia, National Organization for Rare Disorders (NORD)
Chris Haupert MD