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Adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia
rareDiazoxide-resistant hyperinsulism (DRH) is form of congenital isolated hyperinsulinism caused by an abnormal insulin production by b-cells in the pancreas that can be diffuse or focal and is characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia), recurrent episodes of profound hypoglycemia and resistance to medical management with diazoxide
- Identifiers
- MONDO:0017189 Orphanet:276608
- Part of
- Familial hyperinsulinism
- Also known as
- NI-PHH
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