We present a mini-review of cognition in Prader-Willi syndrome. Studies cited include
findings on general ability (IQ), IQ correlates with family members, strengths and …

Prader-Willi syndrome (PWS) is a complex and multisystem neurobehavioral disease, which
is caused by the lack of expression of paternally inherited imprinted genes on …

Prader-Willi syndrome (PWS) is a complex hypothalamic disorder. Features of PWS include
hyperphagia, hypotonia, intellectual disability, and pituitary hormone deficiencies. The …

Although motor problems in Prader–Willi syndrome (PWS) are prominent in infants, and
continue into childhood and adulthood, there is little insight into the factors important for …

Prader-Willi syndrome (PWS) is a rare genetic disorder caused by the loss of imprinted gene
expression on the paternal chromosome 15q11-q13. PWS is characterized by varying …

Prader-Willi syndrome (PWS) is a rare neurodevelopmental and genetic disorder that is
characterized by various expression of endocrine, cognitive and behavioral problems …

Major advances have been made in the identification of genetic neurodevelopmental
disorders and psychological (dis) functioning among persons with intellectual disabilities …

Technological advances in genetic testing have led to a rapid increase in the identification of
causative genetic mutations in individuals with intellectual disability. Beginning in the 1970s …

Prader–Willi syndrome (PWS) is a genetic disorder with obesity, developmental delay, short
stature, and behavioral abnormalities. The study aimed to assess the functional …

This thesis focuses on motor development in infants with Prader-Willi syndrome (PWS) and
the effect of child-specific physical training combined with growth hormone (GH) treatment …