Velocardiofacial Syndrome (VCFS) is a genetic disorder caused by a deletion of a small segment of chromosome 22. It is characterized by a range of physical and developmental features, including heart defects, cleft palate, and facial differences such as a long face and prominent nose. Individuals with VCFS may also experience learning difficulties and behavioral issues. The syndrome is often associated with other health problems, such as immune system deficiencies and psychiatric disorders. Early diagnosis and intervention can help manage symptoms and improve quality of life. Genetic counseling is recommended for affected families to understand the condition better.