Ontology highlight
ABSTRACT: Context
Prader-Willi syndrome (PWS) is a rare, genetic, multisymptom, neurodevelopmental disease due to lack of the expression of the paternal genes in the q11 to q13 region of chromosome 15. The main characteristics of PWS are muscular hypotonia, hyperphagia, obesity, behavioral problems, cognitive disabilities, and endocrine deficiencies, including growth hormone (GH) deficiency. Sleep apnea and abnormal sleep patterns are common in PWS. GH treatment might theoretically have a negative impact on respiration.Objective
Here we present the effect of GH treatment on polysomnographic measurements.Methods
Thirty-seven adults, 15 men and 22 women, with confirmed PWS were randomly assigned to 1 year of GH treatment (n = 19) or placebo (n = 18) followed by 2 years of GH tr
SUBMITTER: Shukur HH
PROVIDER: S-EPMC8372636 | biostudies-literature | 2021 Aug
REPOSITORIES: biostudies-literature