syndrome

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Related to WAGR syndrome: Velocardiofacial syndrome, Wilms tumor, Turner syndrome, Prader Willi syndrome
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Caroline has WAGR syndrome (a rare genetic syndrome in which there is a predisposition to several conditions including certain malignancies, eye abnormalities, and/or mental retardation).
In Ella's case, her aniridia results from a rare chromosome disorder called WAGR syndrome that affects one in 800,000 babies.
Reaching OUT-The WAGR/Aniridia Network" is a newsletter dedicated to offering support and providing information to families affected by WAGR Syndrome.
Three-year-old Ella Chapple has no irises, a condition called aniridia which, in her case, results from a chromosome disorder called WAGR syndrome that affects one in 800,000 babies.