Hyperinsulinemic hypoglycemia in children

Annales d'Endocrinologie

Volumn 65, Issue 1, 2004, Pages 96-98

  de Lonlay, P ^a   Giurgea, I ^a   Robert, J J ^a   Fournet, J C ^a   Touati, G ^a   Nihoul Fekete C ^a   Brunelle, F ^a   Jaubert, F ^a   Rahier, J ^a   Sempoux, C ^a   Junien, C ^a   Saudubray, J M ^a   Dunne, M ^a   Otonkoski, T ^a   Ribeiro, M ^a   Bellane Chantelot C ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

2 OXOGLUTARIC ACID; ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATE; AMINO ACID; CALCIUM ANTAGONIST; DIAZOXIDE; GLUCAGON; GLUCOKINASE; GLUCOSE; GLUCOSE 6 PHOSPHATE; GLUTAMIC ACID; INSULIN; NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; SOMATOSTATIN; SULFONYLUREA DERIVATIVE;

CHILD; CHILDHOOD DISEASE; CLINICAL FEATURE; CONFERENCE PAPER; DISEASE SEVERITY; GLUCOSE BLOOD LEVEL; HUMAN; HYPERINSULINEMIA; HYPOGLYCEMIA; INSULIN BLOOD LEVEL; LABORATORY TEST; MUNCHAUSEN SYNDROME;

EID: 2342597867     PISSN: 00034266     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-4266(04)95640-5     Document Type: Conference Paper

References (24)

1. Brunelle F, Negre V, Barth MO, et al. Pancreatic venous samplings in infants and children with primary hyperinsulinism. Pediatr Radiol 1989; 19: 100-3.
2. Clayton PT, Eaton S, Aynsley-Green A, et al. Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion. J Clin Invest 2001; 108: 457-65.
3. Cornblath M, Schwartz R, Aynsley-Green A, Lloyd JK. Hypoglycemia in infancy: the need for a rational definition. Pediatrics 1990; 85: 834-7.
4. De Lonlay P, Fournet JC, Rahier J, et al. (1997). Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy. J Clin Invest 100: 802-7.
5. De Lonlay-Debeney P, Poggi-Travert F, Fournet JC, et al. (1999). Clinical features of 52 neonates with hyperinsulinism. N Engl J Med 340: 1169-75.
6. Dershewitz R, Vestal B, Maclaren N, Cornblath M (1976). Malicious insulin administration resulting in transient hepatomegaly and hypoglycemia. Am J Dis Child 130: 998-9.
7. Dubois J, Brunelle F, Touati G, etal. (1995). Hyperinsulinism in children: diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases. Pediatr Radiol 25: 512-6.
8. Glaser B, Kesavan P, Heyman M, et al. (1998). Familial hyperinsulinism caused by an activating glucokinase mutation. N Engl J Med 338: 226-30.
9. + ATP channels in persistent hyperinsulinemic hypoglycaemia of infancy. Nature Med 2: 1344-7.
10. Kukuvitis A, Deal C, Arbour L, Polychronakos C (1997). An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus. J Clin Endocrinol Metab 82: 1192-4.
11. Leibowitz G, Glaser B, Higazi AA, Salameh M, Cerasi E, Landau H (1995). Hyperinsulinemic hypoglycemia of infancy (nesidioblastosis) in clinical remission: high incidence of diabetes mellitus and persistent β-cell dysfunction at long-term follow-up. J Clin Endocrinol Metab 80: 386-92.
12. Lindley KJ, Dunne MJ, Kane C, et al. (1996). Ionic control of β-cell function in nesidioblastosis. A possible therapeutic role for calcium channel blockade. Arch Dis Child 74: 373-8.
13. Nestorowicz A, Inagaki N, Gonoit T, et al. (1997). A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism. Diabetes 46: 1743-8.
14. Nestorowicz A, Wilson BA, Schoor KP, et al. (1996). Mutations in the sulfonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews. Hum Mol Genet 5: 1813-22.
15. Pagliara AS, Karl IE, Haymond M, Kipnis DM (1973) Hypoglycemia in infancy and childhood. Part I. J Pediatr 82: 365-79.
16. Rahier J, Fälts K, Münterfering H, Becker K, Gepts W, Falkmer S (1984) The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: deficiency of pancreatic D cells or hyperactivity of β-cells? Diabetologia 26: 282-9.
17. Rahier J, Sempoux C, Fournet JC, et al. (1998). Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's role. Histopathology 32: 15-9.
18. Sempoux C, Guiot Y, Lefevre A, et al. (1998). Neonatal hyperinsulinemic hypoglycemia: heterogeneity of the syndrome and keys for differential diagnosis. J Clin Endocrinol Metab 83: 1455-61.
19. Stanley CA, Lieu YK, Hsu BY, et al. (1998). Hyperinsulinemia and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene. N Engl J Med 338: 1352-7.
20. Thomas P, Ye Y, Lightner E (1996) Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet 5: 1809-12.
21. Thomas PM, Cote GJ, Wohllk N, et al. (1995). Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science 268: 426-9.
22. Verkarre V, Fournet JC, de Lonlay P, et al. (1998). Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. J Clin Invest 102: 1286-91.
23. Volpe JJ (1995). Hypoglycemia and brain injury. In Volpe JJ, ed. Neurology of the Newborn. Philadelphia: Saunders Co., 467-89.
24. Zammarchi E, Filippi L, Novembre E, Donati MA (1996). Biochemical evaluation of a patient with a familial form of leucine-sensitive hypoglycemia and concomitant hyperammonemia. Metabolism 45: 957-60.