What is WAGR Syndrome - 11p Deletion Syndrome

WAGR Syndrome - 11p Deletion Syndrome is a rare genetic disorder caused by the deletion of a small piece of chromosome 11. This condition is characterized by several key features, including Wilms tumor (a type of kidney cancer), aniridia (partial or complete absence of the iris), genitourinary anomalies (abnormalities in the urinary and genital systems), and intellectual disability.

Individuals with WAGR Syndrome may also experience other health issues such as developmental delay, behavioral problems, and obesity. The severity and specific symptoms can vary widely among affected individuals.

Early diagnosis and intervention are crucial for managing the condition and providing appropriate medical care. Genetic testing can confirm the presence of the 11p deletion, and regular screenings are necessary to detect and treat associated conditions, particularly Wilms tumor.

While there is no cure for WAGR Syndrome, treatment focuses on addressing the individual's specific needs and managing associated health concerns. This often involves a multidisciplinary approach, including medical specialists, therapists, and support services.