Summary :
Beckwith–Wiedemann syndrome (BWS) is a disorder of growth
regulation characterized by macrosomia, macroglossia and
developmental abnormalities with a predisposition to tumour
development. The diagnosis of Beckwith-Wiedemann
syndrome may be missed because of variable or incomplete
clinical expression. Here we present a case of a newborn
delivered at BIRDEM (Bangladesh Institute of Research and
Rehabilitation in Diabetes, Endocrine and Metabolic
Disorders) General Hospital, presenting with macrosomia,
macroglossia and hypoglycaemia. The baby also had umbilical
hernia and asymmetry of limbs. The case is presented in order
to create further awareness and to highlight the peculiarity of
management of this rare disorder.
Keywords: Beckwith–Wiedemann Syndrome, Developmental
abnormalities.