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18 Possible Causes for Hyperinsulinemic Hypoglycaemia

  • Leucine-induced Hypoglycemia

    hypoglycaemia of infancy H01267 Familial hyperinsulinemic hypoglycemia Pathway hsa00010 Glycolysis / Gluconeogenesis hsa00071 Fatty acid degradation hsa00471 D-Glutamine[genome.jp] Category Inherited metabolic disease Brite Human diseases [BR: br08402 ] Congenital disorders of metabolism Other congenital disorders of metabolism H01267 Familial hyperinsulinemic[genome.jp] [BR: br08403 ] 05 Endocrine, nutritional or metabolic diseases Endocrine diseases Other disorders of glucose regulation or pancreatic internal secretion 5A45 Persistent hyperinsulinemic[genome.jp]

  • Nesidioblastosis

    Otherwise, the syndrome of hyperinsulinemic hypoglycaemia with nesidioblastosis after Roux-en-Y gastric bypass has been previously reported and it is controversial.[endocrine-abstracts.org] Background: Postprandial hyperinsulinemic hypoglycaemia due to nesidioblastosis is a significant and debilitating complication after Roux-en-Y gastric bypass surgery (RYGB[endocrine-abstracts.org]

  • Postoperative Pancreatitis

    "Partial elective pancreatectomy is curative in focal form of permanent hyperinsulinemic hypoglycaemia in infancy: A report of 45 cases from 1983 to 2000."[surgeryencyclopedia.com]

  • Insulinoma

    METHODS: In this retrospective study, medical records of patients admitted with endogenous hyperinsulinemic hypoglycaemia were retrieved.[ncbi.nlm.nih.gov] Davi MV, Pia A, Guarnotta V, et al, 2016 The treatment of hyperinsulinemic hypoglycaemia in adults: an update. J Endocrinol Invest 40: 9-20. 7.[hormones.gr] BACKGROUND & OBJECTIVES: Since our previous study in 2006, several new modalities for localization of cause of endogenous hyperinsulinemic hypoglycaemia such as multiphasic[ncbi.nlm.nih.gov]

  • Maturity-Onset Diabetes of the Young

    Other GCK mutations result in over-secretion of insulin and present with hyperinsulinemic hypoglycaemia.[diapedia.org]

  • Congenital Disorder of Glycosylation Type 1B

    Managed early in life with treatment Chronic and requires lifelong management Life-threatening with no curative treatments Congenital Disorder of Glycosylation (CDG) is a group of genetic disorders that affects many body systems. More than 75 conditions of CDG have been described, all with defects of[…][evolvegene.com]

  • Multiple Endocrine Neoplasia

    On investigation, she was found to have hyperinsulinemic hypoglycaemia.[ncbi.nlm.nih.gov] Under observation, she was detected to have recurrent hypoglycaemia during the episodes of seizures.[ncbi.nlm.nih.gov]

  • Multiple Endocrine Neoplasia Type 1

    On investigation, she was found to have hyperinsulinemic hypoglycaemia.[ncbi.nlm.nih.gov] Under observation, she was detected to have recurrent hypoglycaemia during the episodes of seizures.[ncbi.nlm.nih.gov]

  • Hawkinsinuria

    Hypoglycaemia Type 1, ABCC8 Gene Analysis Familial Hyperaldosteronism Type 1, CYP11B2 Familial Hyperlepterodenosis (Glucocorticoid Correctable Aldosteronism) Type 3, KCNJ5[nextgenetic.com] Isolated Hypoparathyroidism, PTH Gene Analysis Familial Isolated Hypoparathyroidism, GCM2 Gene Analysis Familial Isolated Pituitary Adenoma (FIPA), AIP Gene Analysis Familial Hyperinsulinemic[nextgenetic.com]

  • Pancreatectomy

    "Partial elective pancreatectomy is curative in focal form of permanent hyperinsulinemic hypoglycaemia in infancy: A report of 45 cases from 1983 to 2000."[surgeryencyclopedia.com] “Partial elective pancreatectomy is curative in focal form of permanent hyperinsulinemic hypoglycaemia in infancy: A report of 45 cases from 1983 to 2000.”[encyclopedia.com]

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