Beckwith-Wiedemann syndrome in a newborn

T Eghbalian

Journal of Inflammatory Diseases

The Official Journal of Qazvin University of Medical Sciences

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Beckwith-Wiedemann syndrome in a newborn

Author(s):

T Eghbalian^,*

Journal of Inflammatory Diseases:Vol. 8, issue 4; 93-97

Article type:Case Report

How to Cite:T EghbalianBeckwith-Wiedemann syndrome in a newborn.J Inflamm Dis.8(4):e155103.

Abstract

Abstract Beckwith-Wiedemann Syndrome is a congenital growth disorder with unknown etiology which correlates with a number and genetic disorders. The prevalence of this syndrome is 1/15000 live birth and the mortality rate is 20% due to complication of prematurity, emphalocele, macroglossia, neonatal hypoglycemia and rarely cardiomyopathy. The basis for diagnosis includes at least two major and one minor criteria. This article presents a 7 hours old neonate with emphalocele, macroglossia and late neonatal hypoglycemia. Having diagnosed as BWS, the patient underwent for repair of abdominal wall defect, correction of hypoglycemia and abdominal sonography to assess the embryonal tumors. A serum insulin level measurement plus an isotope scan on pancreas to determine the cause of hypoglycemia were requested.

Keywords

Keywords: Medical Genetics

Beckwith-Wiedemann

Infancy and Childhood Mortality

Premature Infant

Neonatal Abnormalities

Hypoglycemia

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