22q11.2 deletion syndrome

22q11.2 deletion syndrome is a genetic condition caused by a small missing piece of chromosome 22. This deletion can lead to a variety of health issues, including heart defects, immune system problems, and developmental delays. Some individuals may also experience learning difficulties, speech delays, and psychiatric conditions. The severity and range of symptoms can vary widely among those affected. Early diagnosis and ongoing medical support can help manage the challenges associated with the syndrome, allowing individuals to lead fulfilling lives despite their difficulties. It is often associated with other names, such as DiGeorge syndrome or velocardiofacial syndrome.