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Fig. 1 | International Journal of Pediatric Endocrinology

Fig. 1

From: Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology

Fig. 1

Regulation of insulin release from pancreas β-cell and site of gene mutations involve in the genetics etiology of HH (SUR1: Sulphonyurea receptor 1; Kir 6.2: Inward rectifier potassium channel 6.2; K: Potassium; MCT1: Monocarboxlase transferase-1; Glu: glucose; P: Phosphorus; PGM1: Phosphoglucomutase 1; PMM2: Phosphomannose-mutase 2; UCP2: Mitochondrial uncoupling protein 2; NH3: Ammonia; GDH: Glutamate dehydrogenase; GLUD1: Glutamate dehydrogenase 1 gene; HADH: Hydroxy-acyl-CoA dehydrogenase; HNF1A and 4A: Hepatocyte nuclear factor 1 and 4; Ca+2: Calcium

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International Journal of Pediatric Endocrinology

ISSN: 1687-9856

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