Beckwith-Wiedemann Syndrome is growth disorder syndrome that can cause physical differences and increase your child’s risk for developing certain childhood cancers. While BWS can’t be cured, there are many medical treatments to correct physical differences and to treat medical conditions. What is Beckwith-Wiedemann Syndrome (BWS)?

Beckwith-Wiedemann syndrome is a genetic disorder commonly characterized by overgrowth. The severity of this disorder varies widely in children and is usually recognized at birth, when a child is born with several features of Beckwith-Wiedemann syndrome. However, few children have all the associated characteristics.

Beckwith–Wiedemann syndrome (/ ˈbɛkˌwɪθ ˈviːdə.mən /; abbreviated BWS) is an overgrowth disorder usually present at birth, characterized by an increased risk of childhood cancer and certain congenital features.

Jan 7, 2022 · Beckwith-Wiedemann syndrome was first described by doctors Bruce Beckwith and Hans Rudolph Wiedemann in the 1960’s. The doctors identified children who had a number of symptoms including body overgrowth, external intestines, enlarged tongues, and low blood sugar.

What is Beckwith-Wiedemann syndrome? Beckwith-Wiedemann syndrome (BWS) is a congenital growth disorder, which means it’s present at birth. BWS has various signs and symptoms, including a large body size at birth and taller-than-average height during childhood, a large tongue, and hypoglycemia (low blood sugar).

Our team at the Beckwith-Wiedemann Syndrome Clinic at Children’s Hospital of Philadelphia (CHOP) offers diagnosis, surveillance and treatment for children with Beckwith-Wiedemann Syndrome (BWS) and related disorders. We work closely with your family and your pediatrician throughout your child’s journey.

What is BWS? Beckwith-Wiedemann syndrome (BWS) is a genetic disorder, characterized by overgrowth in certain areas of the body. BWS has a wide range of symptoms and severity. Many features of BWS become less obvious as children get older. Many adults have normal growth and appearance. Children with BWS may have a range of the following features:

• Children with BWS can live full, healthy lives. What is BWS? • Beckwith Wiedemann syndrome is a condition that is caused by genetic changes in a specific region on chromosome 11. • It occurs in about 1 in 11,000 newborns. • The condition can be inherited, but most often it occurs randomly. What features are associated with BWS?

Beckwith-Wiedemann syndrome (BWS) causes a child to grow rapidly from birth until about age eight. This rapid growth sometimes leads to hemihyperplasia, which is an uneven or asymmetric appearance. In most cases, this becomes less obvious over time and, by adulthood, people with this condition are of average height and appearance.

Beckwith-Wiedemann syndrome may be suspected in children who were born larger than normal (macrosomia), with a birth defect where there is an outpouching of abdominal contents into the belly button (umbilical hernia or omphalocele) or who have a large tongue (macroglossia).