Abstract Beckwith-Wiedemann syndrome (BWS), a disorder of overgrowth is a rare
congenital disease and predispose to embryonal tumors. This syndrome is characterized by …

Beckwith-Wiedemann syndrome affects 1 in approximately 14000 newborns. Here we
present an atypical case of an infant with Beckwith-Wiedemann syndrome with mild facial …

Beckwith‐Wiedemann syndrome (BWS) is a congenital overgrowth syndrome with variable
expression. To define the range and frequency of complications in BWS, we have studied a …

Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …

Abstract Beckwith–Wiedemann Syndrome (BWS) is the most common overgrowth syndrome
in infancy. The characteristic findings are macroglossia, abdominal wall defects, and …

Abstract When Beckwith–Wiedemann syndrome (BWS) is detected prenatally, it is usually
on the basis of macroglossia, exomphalos or enlarged kidneys. We describe a case that …

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 …

Discussion Beckwith-Wiedemann syndrome is a disorder of growth characterized by
macrosomia, macroglossia, visceromegaly, embryonal tumors (eg, Wilms tumor …

Clinical and genetical genetic evaluation and. follow-up of 8 patients with Beckwith-
Wiedemann syndrome. Beckwith Wiedemann syndrome (BWS) is a congenital overgrowth …

Beckwith-Wiedemann syndrome is a rare congenital syndrome, but one of the most common
among overgrowth syndromes. It was described firstly by Beckwith in 1963. The incidence of …