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 presented as gross hepatomegaly and a suspected enlarged pancreas at 20 weeks' gestation, with none of the usual features
Beckwith-Wiedemann Sendromu (BWS); konjenital veya zamanla gelişen karın duvar defektleri, kraniyofa...
© 2019 Wolters Kluwer Health, Inc. All rights reserved. Following the discovery of a fetal hepatic t...
Beckwith Wiedemann Syndrome (BWS) is a rare congenital disease of low prevalence. However, it presen...
Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome, characterized by macrosomia, ...
[[abstract]]Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome, characterized by ...
Beckwith-Wiedemann syndrome is a genetic syndrome characterized by macroglossia, omphalocele, fetal ...
Objectives The diagnosis of Beckwith–Wiedemann syndrome (BWS) typically is made after birth. To our ...
Background: Beckwith-Wiedemann syndrome (BWS) is a rare disorder characterized by macrosomia, macrog...
Antenatal detection of an isolated abdominal cyst was found to be a pancreatoblastoma in a female fe...
This baby was born at term by normal vaginal delivery and weighed 4.14 kg. Antenatal period had been...
A five days old 3.3 kg infant, preterm male was admitted at the neonatal ward MNH five hours after b...
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Beckwith-Wiedemann Syndrome is a congenital disease that is rare and has low prevalence worldwide. I...
Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by gigantism, macroglo...
Beckwith-Wiedemann Sendromu (BWS); konjenital veya zamanla gelişen karın duvar defektleri, kraniyofa...
© 2019 Wolters Kluwer Health, Inc. All rights reserved. Following the discovery of a fetal hepatic t...
Beckwith Wiedemann Syndrome (BWS) is a rare congenital disease of low prevalence. However, it presen...
Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome, characterized by macrosomia, ...
[[abstract]]Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome, characterized by ...
Beckwith-Wiedemann syndrome is a genetic syndrome characterized by macroglossia, omphalocele, fetal ...
Objectives The diagnosis of Beckwith–Wiedemann syndrome (BWS) typically is made after birth. To our ...
Background: Beckwith-Wiedemann syndrome (BWS) is a rare disorder characterized by macrosomia, macrog...
Antenatal detection of an isolated abdominal cyst was found to be a pancreatoblastoma in a female fe...
This baby was born at term by normal vaginal delivery and weighed 4.14 kg. Antenatal period had been...
A five days old 3.3 kg infant, preterm male was admitted at the neonatal ward MNH five hours after b...
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Beckwith-Wiedemann Syndrome is a congenital disease that is rare and has low prevalence worldwide. I...
Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by gigantism, macroglo...
Beckwith-Wiedemann Sendromu (BWS); konjenital veya zamanla gelişen karın duvar defektleri, kraniyofa...
© 2019 Wolters Kluwer Health, Inc. All rights reserved. Following the discovery of a fetal hepatic t...
Beckwith Wiedemann Syndrome (BWS) is a rare congenital disease of low prevalence. However, it presen...