Background: Beckwith–Wiedemann syndrome (BWS) is the most common genetic
overgrowth syndrome characterized by the triad of macroglossia, macrosomia, and …

Abstract Beckwith-Wiedemann Syndrome is a congenital disease that is rare and has low
prevalence worldwide. It presents classically with features of macroglossia, abdominal wall …

ABSTRACT Beckwith-Wiedemann Syndrome (BWS) is an overgrowth anomaly of congenital
origin that has low prevalence. However, among the congenital anomalies of overgrowth, it …

Beckwith-Wiedemann syndrome (BWS) is a congenital disorder with 3 main features—
overgrowth in infancy, macroglossia, and abdominal wall defects. Here, we report on a 5 …

Beckwith-Wiedemann syndrome is a pediatric overgrowth disorder with classical features of
macroglossia, exomphalocele and gigantism. Estimated incidence rate of BWS is 1in 13,700 …

Abstract Beckwith-Wiedemann Syndrome (BWS) is an overgrowth anomaly of congenital
origin that has low prevalence. However, among the congenital anomalies of overgrowth, it …

Beckwith‐Wiedemann syndrome is an inherited disorder most commonly characterized by
prenatal or postnatal overgrowth, macroglossia, omphalocele, unusual earlobe creases, and …

Beckwith Wiedemann syndrome is rare congenital overgrowth syndrome. This syndrome
usually presents in neonates with macroglossia, large birth weight, omphalocele …

Since first described in 1963, Beckwith Weidemann syndrome is increasingly being
recognised as an important genetic overgrowth disorder. With the characteristic diagnostic …

ABSTRACT Beckwith-Wiedemann Syndrome (BWS) is a rare congenital anomaly, with
similar manifestation in both sexes and an approximate prevalence of 1/13,700 live births …