eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | congenital hyperinsulinism |
| Comorbidity | C0020598|hypoglycaemia |
| Sentences | 4 |
| PubMedID- 24228030 | Insulin impairs igfbp-1 gene expression, and, as a consequence, high levels of igfbp-1 are present in diabetes mellitus [10] and low levels are noted during hypoglycaemia in patients with congenital hyperinsulinism [13]. |
| PubMedID- 24616771 | congenital hyperinsulinism (chi) leads to severe hyperinsulinaemic hypoglycaemia (hh) in the neonatal, infancy and childhood periods. |
| PubMedID- 24578721 | To date, three tissue-specific isoforms of gck have been characterised 16. an increase in the activity of the enzyme results in hypoglycaemia due to congenital hyperinsulinism (hi, hyperinsulinaemia of infancy). |
| PubMedID- 23813352 | Successful subcutaneous glucagon use for persistent hypoglycaemia in congenital hyperinsulinism. |
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