Obesity is a complex multifactorial disorder with genetic and environmental factors. There is
an increase in the worldwide prevalence of obesity in both developed and developing …

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 …

Prader–Willi syndrome (PWS) is a genetic disorder caused by the lack of expression of
genes on the paternally inherited chromosome 15q11. 2-q13 region. The three main genetic …

Prader–Willi syndrome (PWS) is a complex multisystem disorder due to the absent
expression of the paternally active genes in the PWS critical region on chromosome 15 …

Abstract Context Prader–Willi syndrome (PWS) is characterized by lack of appetite control
and hyperphagia, leading to obesity. Pharmacological options for weight management are …

Background Obesity and lack of physical activity are frequently reported in persons with
intellectual disability (ID) or autism spectrum disorder (ASD). We hypothesised a higher …

Prader-Willi syndrome (PWS) is a complex genetic disorder with implications on the
endocrine and neurologic systems, metabolism, and behavior. Early in life, PWS is …

Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean
body mass, muscular hypotonia, mental retardation, behavioral abnormalities, dysmorphic …

Abstract Prader-Willi Syndrome (PWS) is a multi-system genetically determined
neurodevelopmental disorder and the commonest cause of syndromal obesity. The …

Prader-Willi syndrome (PWS) is a genetic disorder caused by the absence of gene
expression in the 15q11. 2-q13 paternal chromosome. Patients with PWS develop …