Belgian Genetic Tests database
Hyperinsulinism due to INSR deficiency
| Name: |
Hyperinsulinism due to INSR deficiency
|
| Description: |
A rare autosomal dominant form of familial hyperinsulinism characterized clinically by postprandial hypoglycemia, fasting hyperinsulinemia, and an elevated serum insulin-to-C peptide ratio, and a variable age of onset.
|
| ORPHAcode: |
263458
|
| Synonyms: |
Hyperinsulinemic hypoglycemia due to INSR deficiency
Hyperinsulinemic hypoglycemia due to insulin receptor deficiency
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| XREF(s): | |
| Analyte(s): | |
| Created: |
13 May 2019 - 01:02
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| Changed: |
22 Jun 2023 - 16:14
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