Obesity is a growing public health problem in many developed countries, although similar
trends are increasingly being described in some developing nations. The genetic …

Abstract Purpose of Review Prader–Willi syndrome (PWS) is a rare and complex genetic
disorder with multiple effects on the metabolic, endocrine, and neurological systems, as well …

Objectives Prader-Willi syndrome (PWS) significantly impacts health-related quality of life;
however, its relational and existential aspects remain unknown in Italian clinical and social …

Introduction Prader–Willi Syndrome (PWS) is a rare genetic condition, which affects one in
25,000 births and results in various phenotypes. It leads to a wide range of metabolic and …

Several lines of evidence indicate that immune-inflammatory alterations are widely observed
in various mental disorders. Genetic syndromes with high risk of psychiatric disorders may …

Objective: To explore motor praxis in adults with Prader–Willi syndrome (PWS) in
comparison with a control group of people with intellectual disability (ID) and to examine the …

Prader–Willi syndrome (PWS) is a genetic disorder produced by a lack of expression of
paternally derived genes in the 15q11–13 region. Research has generally focused on its …

We compared body composition, biochemical parameters, motor function, and brain neural
activation in 27 adults with Prader–Willi syndrome and growth-hormone deficiency versus …

Although various studies have investigated symptoms of autism spectrum disorder (ASD) in
Prader–Willi syndrome (PWS), little is known about the consequences of these symptoms …

Hyperorality is a distinctive feature of the behavioral variant of frontotemporal dementia
(bvFTD), but little is known about its significance in early-stage disease. This study …