Skip to main content

Advertisement

Log in

Clinical and genetic features of permanent neonatal diabetes mellitus

  • Original Article
  • Published:
International Journal of Diabetes in Developing Countries Aims and scope Submit manuscript

Abstract

Neonatal diabetes mellitus (NDM) is one of the most unusual and exceptional type of diabetes that occurs in infants before the age of 6 months. Transient neonatal diabetes mellitus (TNDM) and permanent neonatal diabetes mellitus (PNDM) are identified clinically. The study conducted was a retrospective cohort study by selecting eight children with neonatal diabetes mellitus between March 2009 and February 2012. The study was presented to King Abdul Aziz University Hospital, in Jeddah, Saudi Arabia. Mutational analysis was performed retrospectively to identify phenotype and genotype characteristics. All patients had NDM and the first symptoms were observed during 1 to 17 weeks of birth, with five males and three females. None of them showed dysmorphic features, seizures, or developmental delay. The timespan of symptoms reported by parents before diagnosis ranged from 3 to 10 days with mean duration of 5.6 days. In two patients (25 %), genetic studies revealed positive mutations, with one patient depicting KCNJ11 mutation and the other had an INS mutation additional screening for ABCC8 and FOXP3 mutations were negative. All patients showed permanent NDM and no transient NDM or the remission at any stage of the disease was observed. Neonatal diabetes is a rare medical condition which needs to be differentiated from transient neonatal hyperglycemia. The medical practitioners should look for molecular basis of neonatal diabetes in order to treat it as it will lead to proper treatment with an appropriate therapy.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Brook C, Clayton P, Brown R (eds). Brook's clinical pediatric endocrinology. John Wiley & Sons; 2009. Retrieved from: http://books.google.co.uk/books?hl=en&lr=&id=sIJETX3z_4IC&oi=fnd&pg=PR6&dq=Diabetes+Mellitus+in:+Endocrinology+6th+edition+&ots=w0dGeonjjx&sig=nN0go77l1EkgeVPoPhGIhvqFrBo#v=onepage&q=Diabetes%20Mellitus%20in%3A%20Endocrinology%206th%20edition&f=false

  2. Hattersley A, Bruining J, Shield J, Njolstad P, Donaghue K. ISPAD clinical practice consensus guidelines 2006–2007. The diagnosis and management of monogenic diabetes in children. Pediatr Diabetes. 2006;7:352–60. doi:10.1111/j.1399-5448.2006.00217.x/abstract.

    Article  PubMed  Google Scholar 

  3. Polak M, Shield J. Neonatal and very-early-onset diabetes mellitus. Semin Neonatol. 2004;9:59–65. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/15013476

  4. Rica I, Luuriaga C, Peres de Nanclares G, Estalella I, Aragones A, et al. The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities. Diabet Med. 2007;24:707–13. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/17490422.

  5. Stoy J, Greeley S, Paz V, Ye H, Pastore A, Skowron K, et al. Diagnosis and treatment of neonatal diabetes: an United States experience. Pediat Diabet. 2008;9:450–9. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/18662362

  6. Clement J, Kunjilwar K, Gonzalez G, Schwanstecher M, Panten U, Aguilar- Bryan L, Bryan J. Association and stoichiometry of KATP channel subunits. Neuron 1997;18:827–838. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/9182806

  7. Stanik J, Gasperikova D, Paskova M, Barak L, Javorkova J, Jancova E, et al. Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriers. J Clin Endocrinol Metab. 2007;92:1276–1282. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/17213273

  8. Pearson E, Flechtner I, Njolstad P, Malecki M, Flanagan S, Larkin B, Ashcroft F, et al. Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. N Engl J Med. 2006;355:467–477. Retrieved from:http://www.nejm.org/doi/full/10.1056/NEJMoa061759

  9. Inoue H, Ferrer J, Warren-Perry M, Zhang Y, Millns H, Turner RC, et al. Sequence variants in the pancreatic islet _-cell inwardly rectifying K_ channel Kir6.2 (Bir) gene: identification and lack of role in Caucasian patients with NIDDM. Diabetes. 1997;46:502–507. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/9032109

  10. Wildin R, Ramsdell F, Peake J, Faravelli F, Casanova J, Buist N, et al. X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy. Nat Genet. 2001;27:18–20. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/11137992

  11. Schwitzgebel V, Mamin A, Brun T, Ritz-Laser B, Zaiko M, Maret A, et al. Agenesis of human pancreas due to decreased half-life of insulin promoter factor 1. J Clin Endocrinol Metab. 2003;88:4398–4406. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/12970316

  12. Nestorowicz A, Wilson B, Schoor K, Inoue H, Glaser B, Landau H, et al. Mutations in the sulfonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews. Human Mol Genet. 1996;11:1813–1822. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/8923011

  13. Gloyn A, Pearson E, Antcliff J et al. Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes. N Engl J Med. 2004;350:1838–49. Retrieved from:http://www.ncbi.nlm.nih.gov/pubmed/15115830

Download references

Acknowledgments

We are especially thankful to Professor Sian Ellard, who is a Consultant at Molecular Genetics Laboratory, of the Royal Devon and Exeter NHS Healthcare Trust, Barrack Road, Exeter, UK. Moreover, we are also grateful to Andrew Parrish, the Genetic Technologist and Jayne Houghton, the Clinical Scientist, for their excellent assistance and support in the successful accomplishment of this work.

Conflicts of Interest

None

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Abdulmoein E. Al-Agha.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Al-Agha, A.E., Ahmad, I.A. Clinical and genetic features of permanent neonatal diabetes mellitus. Int J Diabetes Dev Ctries 36, 18–22 (2016). https://doi.org/10.1007/s13410-015-0398-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13410-015-0398-9

Keywords

Navigation