DiGeorge Syndrome is a genetic disorder caused by a deletion of a small piece of chromosome 22. This condition can lead to a variety of health issues, including heart defects, immune system problems, and developmental delays. Individuals with DiGeorge Syndrome may also experience difficulties with learning and may have distinctive facial features. Symptoms can vary widely among those affected, making diagnosis challenging. Common signs include low calcium levels, speech delays, and behavioral issues. Early intervention and treatment can help manage symptoms and improve quality of life for individuals with DiGeorge Syndrome.