Ontology highlight
ABSTRACT: Context
Recombinant human GH (rhGH) therapy in Prader-Willi syndrome (PWS) has been used by the medical community and advocated by parental support groups since its approval in the United States in 2000 and in Europe in 2001. Its use in PWS represents a unique therapeutic challenge that includes treating individuals with cognitive disability, varied therapeutic goals that are not focused exclusively on increased height, and concerns about potential life-threatening adverse events.Objective
The aim of the study was to formulate recommendations for the use of rhGH in children and adult patients with PWS.Evidence
We performed a systematic review of the clinical evidence in the pediatric population, including randomized controlled trials, comparative observational studi
SUBMITTER: Deal CL
PROVIDER: S-EPMC3789886 | biostudies-literature | 2013 Jun
REPOSITORIES: biostudies-literature