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Am J Emerg Med ; 54: 327.e5-327.e6, 2022 Apr.
Article in English | MEDLINE | ID: mdl-34756479

ABSTRACT

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.


Subject(s)
Diabetes Mellitus, Type 1 , Diabetic Ketoacidosis , Hyperglycemic Hyperosmolar Nonketotic Coma , Infant, Newborn, Diseases , Coma , Diabetes Mellitus, Type 1/complications , Diabetic Ketoacidosis/complications , Diabetic Ketoacidosis/diagnosis , Humans , Hyperglycemic Hyperosmolar Nonketotic Coma/complications , Hyperglycemic Hyperosmolar Nonketotic Coma/diagnosis , Infant , Infant, Newborn , Insulin/therapeutic use
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