Beckwith-Wiedemann Syndrome (BWS) is a genetic disorder that affects growth and development. It is characterized by features such as overgrowth, an enlarged tongue, and abdominal wall defects. Children with BWS may also have an increased risk of certain tumors, particularly in early childhood. The condition is caused by changes in genes that regulate growth, often involving the 11p15 chromosomal region. Diagnosis of BWS typically involves physical examination and genetic testing. Management may include regular monitoring for tumors and addressing any physical abnormalities. Early intervention and supportive care can help improve outcomes for individuals with Beckwith-Wiedemann Syndrome.