In:
Journal of Diabetes, Wiley, Vol. 12, No. 1 ( 2020-01), p. 21-24
Abstract:
Highlights Inactivating mutations of the ABCC8 gene usually cause hyperinsulinemic hypoglycemia. We report a family in which people with the inactivating mutation have progressed hyperinsulinemic hypoglycemia to hyperglycemia. Treatment with incretin‐related drugs might be a useful therapeutic approach to hyperglycemia in people with the inactivating mutation.
Type of Medium:
Online Resource
ISSN:
1753-0393
,
1753-0407
DOI:
10.1111/1753-0407.12990
Language:
English
Publisher:
Wiley
Publication Date:
2020
detail.hit.zdb_id:
2485432-3