Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease hyperinsulinism
Symptom C0020598|hypoglycemia
Sentences 19
PubMedID- 22759688 This case illustrates the complex relationship between seizures and hypoglycemia in hyperinsulinism-hyperammonemia syndrome that can create diagnostic difficulties.
PubMedID- 21086579 The hypoglycemia is associated with an endogenous hyperinsulinism, also observed in a rare endocrine pathology, the insulinoma.
PubMedID- 26316438 Unlike other congenital fatty acid oxidation defects, short-chain l-3-hydroxyacyl-coa (schad, hadh) deficiency is characterised by hypoglycemia with hyperinsulinism in the neonatal or infancy periods.
PubMedID- 26392140 Diazoxide is used to treat severe hypoglycemia due to hyperinsulinism of infancy.
PubMedID- 23275527 Context: hypoglycemia due to congenital hyperinsulinism (hi) is caused by mutations in 9 genes.
PubMedID- 22584561 hypoglycemia due to endogenous hyperinsulinism (eh) is diagnosed in a symptomatic patient with low levels of plasma glucose concomitant with elevated plasma insulin and c-peptide.
PubMedID- 25972930 Diazoxide is the medication of choice for the treatment of hypoglycemia due to hyperinsulinism during the neonatal period.
PubMedID- 24728168 In this paper, we describe two cases of hypoglycemia associated with endogenous hyperinsulinism, whose causes are uncommon in clinical practice, and review important aspects of the diagnosis and treatment of hyperinsulinemic hypoglycemia.
PubMedID- 25943194 In the first 24 hours, the patient presented with hypoglycemia attributed to hyperinsulinism and was treated with diazoxide.
PubMedID- 24275620 But hypoglycemia due to hyperinsulinism, especially genetic causes, continued to be associated with brain injury.
PubMedID- 21536946 Inactivating mutations of the β-cell atp-sensitive k+ channel (katp channel) are the most common cause of hypoglycemia due to congenital hyperinsulinism (1).
PubMedID- 24639276 The hypoglycemia was attributable to hyperinsulinism and was treated with diazoxide and chlorothiazide.
PubMedID- 24621811 In comparison with the severe hypoglycemia characteristic of patients with congenital hyperinsulinism (chi) secondary to loss of katp channel function (reviewed in ), sur1−/− mice, with the equivalent channel deficit, show near normal glucose homeostasis unless stressed , , , .
PubMedID- 24075522 Discussion: nesidioblastosis is a rare pathology, but it must be present in the differential diagnosis of hypoglycemia symptoms with endogenous hyperinsulinism in adults, once the intake of sulfonylureas and possible pancreatic neoformations have been ruled out.
PubMedID- 19952738 Studies of the cause of hypoglycemic brain damage and the relationship of hypoglycemia to disorders associated with hyperinsulinism have aided in our understanding of this common clinical finding.
PubMedID- 26180531 Congenital hyperinsulinism (chi) leads to hypoglycemia in infants and children due to inappropriately elevated insulin levels.
PubMedID- 23274908 Deletion of foxa2 in all β-cells caused severe neonatal hypoglycemia with relative hyperinsulinism (45) that was at least partly attributable to defects in katp channels (46).
PubMedID- 25870695 A high level of glucose should trigger more attention as rebound hyperinsulinism could appear with subsequent severe hypoglycemia 4.
PubMedID- 25618267 Stress-related hyperinsulinism (hi) may lead to recalcitrant hypoglycemia for weeks or months following perinatal stress, often in premature newborn infants.

Page: 1