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Updated: Mar 11, 2026

Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
Neonatal Diabetes: A Case Series
Ramaswamy Ganesh1, Natarajan Suresh, Thiruvengadam Vasanthi
1Departments of Pediatrics and *Endocrinology, Kanchi Kamakoti CHILDS Trust Hospital and The CHILDS Trust Medical Research Foundation, Chennai, Tamil Nadu, India. Correspondence to: Dr Ramaswamy Ganesh, Consultant Pediatrician, Kanchi Kamakoti CHILDS Trust Hospital, Chennai 600 034, India. ganeped79@rediffmail.com.
Background:
Neonatal diabetes mellitusis a rare disorder with an incidence of 1 in 2,60,000 live births.
Methods:
Retrospective analysis of clinical and genetic profile of children admitted with neonatal diabetes mellitus in a tertiary-care hospital in Chennai, India over 11 years.
Results:
Ten children were diagnosed with neonatal diabetes of whom 9 had permanent neonatal diabetes mellitus. The age range at onset was from 3 days- 5 months. Of the 9 children, KCNJ11 gene mutation was positive in one, and ABCC 8 and INS gene mutation in two children each. Children with KCNJ11 and ABCC 8 gene mutations were switched over to oral sulfonyl urea therapy.
Conclusion:
Few genotypes causing NDM can be managed effectively with oral sulfonyl ureas.
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