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Intern Med ; 63(15): 2153-2156, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-38171878

ABSTRACT

Glycogen storage disease type 1a (GSD-1a) is a rare congenital disease. Recently, life expectancy with GSD-1a has been improved by its early diagnosis and management. Complications of diabetes with GSD-1a are extremely rare. The optimal treatment for glucose control using this disease combination remains unclear. The existence of GSD-1a and diabetes can cause both hypoglycemia and hyperglycemia, making glucose control especially problematic. In the present report, α-glucosidase inhibitor (α-GI) and dipeptidyl peptidase-4 (DPP-4) inhibitors improved hyperglycemia without symptoms of hypoglycemia in a patient with diabetes and GSD-1a using intermittent continuous glucose monitoring (isCGM).


Subject(s)
Glycogen Storage Disease Type I , Glycoside Hydrolase Inhibitors , Humans , Glycogen Storage Disease Type I/complications , Glycogen Storage Disease Type I/diagnosis , Glycoside Hydrolase Inhibitors/therapeutic use , Dipeptidyl-Peptidase IV Inhibitors/therapeutic use , Male , Blood Glucose/metabolism , Female , Hypoglycemic Agents/therapeutic use , Adult , Hyperglycemia/complications , Hyperglycemia/diagnosis
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