1. Genetic Variations in Hyperinsulinemic Hypoglycemia: Active versus Inactive Mutations
- Author
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Sabi SH, Alzreqat RK, Almaaytah AM, Masaadeh MM, and Abualhaijaa AK
- Subjects
hyperinsulinemic hypoglycemia ,nesidioblastosis ,glud1 ,hexokinase ,foxa2. ,Specialties of internal medicine ,RC581-951 - Abstract
Salsabeel H Sabi,1 Roaa K Alzreqat,2 Ammar M Almaaytah,3 Majed M Masaadeh,3 Ahmad Khaled Abualhaijaa3 1Basic Sciences Department, The Hashemite University, Zarqa, Jordan; 2Department of Biological Sciences, The Hashemite University, Zarqa, Jordan; 3Department of Pharmaceutical Technology, Jordan University of Science and Technology, Irbid, JordanCorrespondence: Salsabeel H Sabi, Email salsabeel@hu.edu.joAbstract: Hyperinsulinemic Hypoglycemia (HH) is a rare condition that affects newborn children in the postnatal period, represented by dangerously low levels of blood glucose in a persistent manner, which puts the baby at high risk of multiple issues, especially regarding the brain cells if the baby does not take the appropriate medication or have the correct diagnosis. Hyperinsulinemic Hypoglycemia can happen due to an active or inactive mutation in 16 genes responsible for glucose metabolism and insulin secretion (GLUD1, GCK, SLC16A1, HK1, CACNA1D, KCNJ11, ABCC8, FOXA2, HNF1A, HNF4A, HADH, PGM1, UCP2, KCNQ1, PMM2, EIF2S3). These mutations can take place in many forms, either defused or local, affecting several or all pancreatic beta cells respectively. This review summarizes genetic variations diagnosis and treatment of Hyperinsulinemic Hypoglycemia.Keywords: Hyperinsulinemic Hypoglycemia, nesidioblastosis, GLUD1, hexokinase, FOXA2
- Published
- 2024