peer reviewedBeckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by an overgrowth, macroglossia, exomphalos, and predisposition to embryonal tumors. Central nervous abnormalities associated with BWS are rare. We describe a one-day-old Congolese female who presented meningocele associated with BWS phenotype
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Background Beckwith Wiedemann syndrome (BWS) is a clinically variable and genetically heterogeneous ...
Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by an overgrowth, macr...
Copyright © 2014 Sébastien Mbuyi-Musanzayi et al. This is an open access article distributed under ...
Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by gigantism, macroglo...
French Title: Le syndrome De Beckwick-Wiedemann neglige revele par une macroglossie severe The Beckw...
Beckwith-Wiedemann Sendromu (BWS); konjenital veya zamanla gelişen karın duvar defektleri, kraniyofa...
Beckwith–Wiedemann syndrome (BWS) is a rare syndrome and has an estimated incidence of one in 13,700...
Beckwith - Wiedemann syndrome (ICD-10 code: Q 87.3) is a congenital disease characterized by macroso...
Beckwith Wiedemann Syndrome (BWS) is a rare congenital disease of low prevalence. However, it presen...
Introduction: Beckwith-Wiedemann syndrome is an overgrowth syndrome that is characterized by hypogly...
Beckwith-Wiedemann Syndrome is a congenital disease that is rare and has low prevalence worldwide. I...
Background: Beckwith-Wiedemann syndrome (BWS) is a clinically variable and genetically heterogeneous...
The Authors describe a case of Beckwith-Wiedemann syndrome. In this patient marked macroglossia and ...
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Background Beckwith Wiedemann syndrome (BWS) is a clinically variable and genetically heterogeneous ...
Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by an overgrowth, macr...
Copyright © 2014 Sébastien Mbuyi-Musanzayi et al. This is an open access article distributed under ...
Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by gigantism, macroglo...
French Title: Le syndrome De Beckwick-Wiedemann neglige revele par une macroglossie severe The Beckw...
Beckwith-Wiedemann Sendromu (BWS); konjenital veya zamanla gelişen karın duvar defektleri, kraniyofa...
Beckwith–Wiedemann syndrome (BWS) is a rare syndrome and has an estimated incidence of one in 13,700...
Beckwith - Wiedemann syndrome (ICD-10 code: Q 87.3) is a congenital disease characterized by macroso...
Beckwith Wiedemann Syndrome (BWS) is a rare congenital disease of low prevalence. However, it presen...
Introduction: Beckwith-Wiedemann syndrome is an overgrowth syndrome that is characterized by hypogly...
Beckwith-Wiedemann Syndrome is a congenital disease that is rare and has low prevalence worldwide. I...
Background: Beckwith-Wiedemann syndrome (BWS) is a clinically variable and genetically heterogeneous...
The Authors describe a case of Beckwith-Wiedemann syndrome. In this patient marked macroglossia and ...
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Beckwith Wiedemann syndrome is a complex developmental disorder characterized by somatic overgrowth,...
Background Beckwith Wiedemann syndrome (BWS) is a clinically variable and genetically heterogeneous ...