In utero diagnosis of Beckwith-Wiedeman syndrome was made after sonographic
identification of an omphalocele and organomegaly in a term fetus. Although not all possible …

Beckwith‐Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by an
overgrowth, macroglossia, exomphalos, and predisposition to embryonal tumors. Central …

Beckwith–Wiedemann syndrome (BWS) is the most common overgrowth disorder usually
present at birth, characterized by an increased risk of embryonal tumors, such as …

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

Beckwith-Wiedemann syndrome (BWS) is a rare congenital overgrowth syndrome
associated with certain childhood tumours. We present the case of a 36-year-old lady with …

In 1963 Beckwith'presented the necropsy findings of three unrelated children with exompha-
los, macroglossia, hyperplasia of the kidneys and pancreas, and adrenal cytomegaly, and …

This report describes two new cases of BWS. This diagnosis of BWS may be missed
because of variable or incomplete clinical expression. Recognition of such patients is …

Discussion The hong-term survival of patients with Wihms' tumor that is diagnosed early and
treated appropriately is good [1]. Early detection of Wilms' tumor, to which patients with …

Abstract Beckwith Wiedemann Syndrome (BWS) is a rare congenital disease of low
prevalence. However, it presents a high prevalence within the genetic pathologies of …

Abstract Beckwith-Wiedemann Syndrome (BWS) is a rare congenital disorder caused by
alterations to the IGF2 gene. Its incidence has increased with the use of assisted …