Diagnosis and identification of related inherited metabolic disorders in children with hypoglycemia
10.3760/cma.j.issn.2095-428X.2018.20.001
- VernacularTitle:儿童低血糖相关遗传代谢病的诊断与鉴别
- Author:
Xiyu HE
1
;
Yinru LIU
Author Information
1. 中国人民解放军第307医院儿科
- Keywords:
Hypoglycemia;
Inherited metabolic disorders;
Diagnosis;
Child
- From:
Chinese Journal of Applied Clinical Pediatrics
2018;33(20):1521-1526
- CountryChina
- Language:Chinese
-
Abstract:
Hypoglycemia is a common metabolic disorder in children,and its incidence is about 10％.Among them,the incidence of hereditary related diseases is about 1/30 000-10/30 000.More and more genetic diseases leading to hypoglycemia have been discovered in recent years.Children with the disease may have mild nervous system damage at the earliest stage,and liver encephalopathy,respiratory failure,confusion or even death in severe cases.Therefore,more and more attention has been paid to the study of hypoglycemia related genetic diseases,but the diagnosis and differential diagnosis of hypoglycemia has not yet formed an unified consensus.Now,the diagnosis and treatment of this kind of related diseases were summarized in order to provide data for clinical practice.
