What is Beckwith-Wiedemann syndrome?

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.

How is Beckwith-Wiedemann syndrome diagnosed?

BWS may be diagnosed or confirmed shortly after birth based on a thorough clinical evaluation, detection of characteristic physical findings (e.g., increased weight and length, macroglossia, abdominal wall defects), and genetic testing of the BWS critical region.

How common is Beckwith-Wiedemann syndrome?

Beckwith-Wiedemann syndrome affects 1 in 10,500 to 13,700 newborns worldwide. The condition may actually be more common than this estimate because some people with mild symptoms are never diagnosed.

Is there a cure for BWS?

BWS can’t be cured. But medical treatments and other care can help resolve most of BWS’ symptoms. Ask your healthcare provider what medical challenges you and your child may face.

Can Beckwith-Wiedemann syndrome be cured?

Beckwith-Wiedemann syndrome has no cure, but some treatments can help ease its symptoms. The most common Beckwith-Wiedemann syndrome treatments include: Medicine: Some infants require medicine for low blood sugar that persists past their first month.

Is Beckwith-Wiedemann a disability?

Is BWS a developmental disability? Unless a child has had untreated low blood sugar or other medical complication, there’s no indication that Beckwith-Wiedemann Syndrome affects children’s intellectual ability.

Is Beckwith-Wiedemann syndrome diagnosed at birth?

Beckwith-Wiedemann syndrome is a growth disorder that causes large body size, large organs, and other symptoms. It is a congenital condition, which means it is present at birth. The signs and symptoms of the disorder vary somewhat from child to child.

Is Beckwith Wiedemann a disability?