Obesity presents a major health hazard of the 21st century. It promotes co-morbid diseases
such as heart disease, type 2 diabetes, obstructive sleep apnea, certain types of cancer, and …

Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder associated with
a characteristic behavioral phenotype that includes severe hyperphagia and a variety of …

Objective: The objective of the study was to provide recommendations for the diagnosis and
management of Prader-Willi syndrome throughout the life span to guide clinical practice …

Oxytocin (OT), the main neuropeptide of sociality, is expressed in neurons exclusively
localized in the hypothalamus. During the last decade, a plethora of neuroendocrine …

Prader–Willi syndrome (PWS) is a complex neurodevelopmental disorder caused by an
abnormality on the long arm of chromosome 15 (q11–q13) that results in a host of …

Prader-Willi syndrome (PWS) is caused by either the structural loss of material or the
absence of gene expression from the paternally inherited copy of chromosome 15 in the q11 …

Abstract Prader-Willi syndrome (PWS), a neurodevelopmental disorder primarily
characterized by hyperphagia and food preoccupations, is caused by the absence of …

Background The behavioural phenotypes of Prader–Willi (PWS) and Fragile‐X (FraX)
syndromes both comprise repetitive behaviours with differences between the profiles. In this …

Abstract Background Prader–Willi syndrome (PWS) is a rare genetic disorder characterised
by developmental abnormalities leading to somatic and psychological symptoms. These …

Abstract Background Prader–Willi syndrome (PWS) is a genetic syndrome associated with
several physical, cognitive and behavioural characteristics. For many individuals with this …