Constitutional molecular defects are known to play a role in oncogenesis, as shown by the
increased incidence of embryonic cancers in children with Beckwith–Wiedemann syndrome …

Beckwith–Wiedemann syndrome (BWS) is the most common (epi) genetic overgrowth-
cancer predisposition disorder. Given the absence of consensual recommendations or …

The diagnosis of Beckwith-Wiedemann syndrome may be missed because of variable or
incomplete clinical expression. Recognition of such patients is important, however, because …

Objective: Beckwith-Wiedemann Syndrome (BWS) is an overgrowth syndrome associated
with macrosomia, omphalocele, macroglossia, visceromegaly and Wilms tumor (WT). We …

A specific subset of solid childhood tumors—Wilms' tumor, adrenocortical carcinoma,
rhabdomyosarcoma, and hepatoblastoma—is characterized by its association with Beckwith …

Abstract Background Children with Beckwith‐Wiedemann syndrome and idiopathic
hemihypertrophy (BWS/HH) are at increased risk for developing Wilms tumor and screening …

Beckwith–Wiedemann syndrome (BWS) is characterized by cancer predisposition,
overgrowth and highly variable association of macroglossia, abdominal wall defects …

Beckwith-Wiedemann syndrome (BWS) is a congenital cancer-predisposition syndrome
associated with embryonal cancers, macroglossia, macrosomia, ear pits or ear creases, and …

Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably characterized by
neonatal hypoglycemia, macrosomia, macroglossia, hemihyperplasia, omphalocele …

We conducted a follow‐up study on 15 patients with Wiedemann‐Beckwith syndrome (WBS)
to further clarify major and minor diagnostic clinical characteristics and long‐term …