Molecular defects in persistent hyperinsulinemic hypoglycemia in infants
- VernacularTitle:婴幼儿持续高胰岛素血症性低血糖症的分子病因
- Author:
Mengyin CAI
;
Jianping WENG
- Publication Type:Journal Article
- Keywords:
Persistent hyperinsulinemic hypoglycemia in infants;
Molecular defect
- From:
Chinese Journal of Endocrinology and Metabolism
1986;0(04):-
- CountryChina
- Language:Chinese
-
Abstract:
Persistent hyperinsulinemic hypoglycemia in infants is one of the most common causes of persistent hypoglycemia in infants. The knowledge of molecular defects leading to persistent hyperinsulinemic hypoglycemia in infants has been rapidly growing in recent years. According to the responsible genes, this ailment can be divided into five types. However, no molecular defect can be yet found in as many as 50% of the patients.
