22q deletion syndrome, also known as DiGeorge or CATCH 22 syndrome, is a genetic disorder caused by the absence of a small part of chromosome 22. It results in underdevelopment of several body systems including the thymus gland. Common features include cardiac defects, facial abnormalities, cleft palate, low calcium levels, immune deficiency, and learning disabilities. While there is no cure, treatment focuses on managing infections, cardiac issues, and hormone deficiencies through antibiotics, surgery, and supplements. Prognosis depends on severity, but many individuals can live fairly normal lifespans with proper care.