22q11.2 Deletion Syndrome is a genetic disorder caused by the deletion of a small segment of chromosome 22. This condition can lead to a variety of health issues, including heart defects, immune system problems, and developmental delays. Individuals with this syndrome may also experience learning difficulties and behavioral challenges. The symptoms of 22q11.2 Deletion Syndrome can vary widely among affected individuals. Some may have physical features such as a cleft palate or distinctive facial characteristics, while others may have more subtle signs. Early diagnosis and intervention can help manage the symptoms and improve quality of life for those affected.