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 …

Management of Prader-Willi Syndrome is the first book to provide a comprehensive source
of knowledge about Prader-Willi Syndrome and to offer common-sense guidelines for …

Background: Prader-Willi Syndrome (PWS) is a neurodevelopmental genomic imprinting
disorder with lack of expression of genes inherited from the paternal chromosome 15q11 …

Prader-Willi syndrome (PWS) is characterized by severe hypotonia and feeding difficulties in
early infancy, followed in later infancy or early childhood by excessive eating and gradual …

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 …

Prader-Willi syndrome (PWS) is a complex genetic condition characterized by a range of
mental and physical findings, with obesity being the most significant health problem. PWS is …

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 …

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 complex genetic disorder, caused by lack of expression of
genes on the paternally inherited chromosome 15q11. 2-q13. In infancy it is characterized …