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

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 a rare genetic syndrome. The phenotype includes moderate
to intellectual disability, dysmorphia, obesity, and behavioral disturbances (eg, hetero and …

Prader–Willi syndrome (PWS) is now recognized as a genetically determined complex
neurodevelopmental syndrome with distinct characteristics that evolve during early …

Advances in technologies offer new opportunities to collect and integrate data from a broad
range of sources to advance the understanding of rare diseases and support the …

Objectives Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by
maladaptive behaviors, amongst which hyperphagia is a life-long concern for individuals …

Although people with intellectual disabilities are at increased risk for psychiatric disorders,
the type and rate of these problems differ between those with different causes for their …

In early childhood, individuals with Prader‐Willi syndrome (PWS) experience excess weight
gain and severe hyperphagia with food compulsivity, which often leads to early onset morbid …

Now in a fully revised and updated fourth edition, this book remains the most comprehensive
resource on Prader-Willi syndrome (PWS) available on the market. There have been …

Cognitive and behavioural aspects of Prader–Willi syndrome : Current Opinion in Psychiatry
Cognitive and behavioural aspects of Prader–Willi syndrome : Current Opinion in Psychiatry …