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Volume 21, Issue 1
  • ISSN: 1573-3998
  • E-ISSN: 1875-6417

Abstract

Introduction

Neonatal diabetes mellitus (NDM) is characterized by severe hyperglycemia, usually diagnosed in the first few months of an individual’s life. It is a genetic disease and one of the main forms of monogenic diabetes. Changes in different genes have already been associated with NDM, including changes in the gene .

Methods

In this review, we intend to summarize all neonatal diabetes cases caused by mutations reported in the literature. For this purpose, we searched keywords in the literature from PubMed and articles cited by the HGMD database. The search retrieved 84 articles, of which 41 had their full text accessed. After applying the study exclusion criteria, nine articles were included.

Results

Of those articles, we detected thirteen cases of NDM associated with changes in ; the majority in homozygous or compound heterozygous patients. Until now, variants in the gene have been a rare cause of NDM; however, few studies have included the screening of this gene in the investigation of neonatal diabetes.

Conclusion

In this review, we reinforce the importance of the gene inclusion in genetic NGS panels for molecular diagnosis of NDM, and systematic morphological and functional exams of the pancreas when NDM is present.

© 2025 Bentham Science Publishers
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2024-01-29
2025-06-22

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/content/journals/cdr/10.2174/0115733998265866231204070606
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What Do We Know about Neonatal Diabetes caused by PDX1 Mutations?
Curr. Diabetes Rev. 21, E290124226471 (2025); https://doi.org/10.2174/0115733998265866231204070606
/content/journals/cdr/10.2174/0115733998265866231204070606
/content/journals/cdr/10.2174/0115733998265866231204070606
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  • Article Type:     Review Article
Keyword(s): IPF1 gene; MODY4; mutation; Neonatal diabetes; PDX1 gene; PDX1-MODY

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