Hyperosmolar hyperglycemic coma in an infant with neonatal diabetes mellitus

Neonatal diabetes mellitus (NDM) is a rare disease distinct from type 1 diabetes mellitus (T1DM). While T1DM results from autoimmune destruction of pancreatic beta cells, NDM arises from genetic mutations to insulin production and secretion pathways. We present a case of an infant presenting to the...

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Bibliographic Details
Published inThe American journal of emergency medicine Vol. 54; pp. 327.e5 - 327.e6
Main Authors Foughty, Zachary C., Moryan-Blanchard, Kristen, Henkel, Erin B., Gahm, Claire
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.04.2022
Elsevier Limited
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Summary:Neonatal diabetes mellitus (NDM) is a rare disease distinct from type 1 diabetes mellitus (T1DM). While T1DM results from autoimmune destruction of pancreatic beta cells, NDM arises from genetic mutations to insulin production and secretion pathways. We present a case of an infant presenting to the emergency department with shock and poor responsiveness, found to have neonatal DM with hyperosmotic hyperglycemic syndrome (HHS). This report distinguishes NDM from T1DM, illustrating the subtle but clinically significant differences in pathophysiology and implications for initial management of NDM in the emergency department setting.
ISSN:0735-6757
1532-8171
DOI:10.1016/j.ajem.2021.10.026