Neonatal diabetes and protein losing enteropathy: a case report

Citation metadata

Authors: Tamara McMillan, Rose Girgis and Elizabeth A. C. Sellers
Date: Apr. 21, 2016
From: BMC Medical Genetics(Vol. 17, Issue 1)
Publisher: BioMed Central Ltd.
Document Type: Report
Length: 2,034 words

Main content

Abstract :

Background Neonatal diabetes is a rare form of monogenic diabetes with onset in the first six months of life occurring in 1/100,000 to 1/400,000 births. Both permanent and transient forms have been described. Permanent neonatal diabetes results predominantly from mutations in the KCNJ11 and ABCC8 genes. Less frequently, mutations of the GATA6 gene, located on chromosome 18 cause a form of permanent neonatal diabetes resulting from pancreatic hypoplasia or agenesis. Other anomalies associated with mutations of this gene have also been reported, most commonly congenital heart disease. Case presentation We report the case of a Caucasian male infant diagnosed shortly after birth with neonatal diabetes, truncus arteriosus type III, ventricular septal defect, atrial septal defect, an absent gallbladder and a right inguinal hernia. His diabetes resulted from a de novo mutation of the GATA6 gene resulting in pancreatic hypoplasia. At 20 months of age he developed protein losing enteropathy. This has not previously been associated with GATA6 mutations and it is not known if this association is causal. Conclusion The combination of neonatal diabetes and pancreatic agenesis/hypoplasia should alert the clinician to the possibility of a GATA6 gene abnormality. The association of protein losing enteropathy is unique to the reported case. Keywords: Neonatal diabetes, pancreatic hypoplasia, protein losing enteropathy

Source Citation

Source Citation
McMillan, Tamara, et al. "Neonatal diabetes and protein losing enteropathy: a case report." BMC Medical Genetics, vol. 17, no. 1, 2016. Accessed 12 May 2021.
  

Gale Document Number: GALE|A469984865