Application of recombinant human growth hormone in treatment of Prader-Willi syndrome
10.3760/cma.j.issn.2095-428X.2016.08.002
- VernacularTitle:重组人生长激素在Prader-Willi综合征治疗中的应用
- Author:
Xiaohong CHEN
;
Hui YAO
- Publication Type:Journal Article
- Keywords:
Prader-Willi syndrome;
Recombinant human growth hormone;
Insulin-like growth factor-1;
Obesity;
Metabolic syndrome
- From:
Chinese Journal of Applied Clinical Pediatrics
2016;31(8):564-568
- CountryChina
- Language:Chinese
-
Abstract:
Prader-Willi syndrome is a rare genetic disorder characterized by hypotonia,poor feeding in infancy,hyperphagia with evolving obesity,hypogonadism,decreased adult height,and cognitive and behavioral disabilities.Recombinant human growth hormone (rhGH) has been used in treating Prader-Willi syndrome,and it has achieved good results.Several aspects still need to be concerned,including evaluation before rhGH treatment,age at treatment initiation,dosing,monitoring of potential side effects,tolerability,endpoint,response evaluation,use of adjunct therapies,and issues of consent.