Last edited by Dojar
Sunday, August 2, 2020 | History

7 edition of Management of Prader-Willi Syndrome found in the catalog.

Management of Prader-Willi Syndrome

  • 391 Want to read
  • 8 Currently reading

Published by Springer .
Written in English

    Subjects:
  • Congenital diseases & disorders,
  • Medical,
  • Medical / Nursing,
  • Endocrinology & Metabolism,
  • Life Sciences - Genetics & Genomics,
  • Pediatrics,
  • Medical / Pediatrics,
  • Prader-Willi syndrome

  • Edition Notes

    ContributionsMerlin Butler (Editor), Phillip D.K. Lee (Editor), Barbara Y. Whitman (Editor)
    The Physical Object
    FormatHardcover
    Number of Pages550
    ID Numbers
    Open LibraryOL9499089M
    ISBN 100387253971
    ISBN 109780387253978

      Management of Prader-Willi Syndrome brings together the contributions of professionals with considerable expertise in diagnosis and management of PWS. Clinical, social, family, and community issues are explored and management strategies identified. The text presents historical, medical, and genetic information to orient the reader. Prader-Willi California Foundation. First Avenue Suite San Diego, CA () () Toll-free within CA. [email protected]

    Prader-Willi Syndrome. Prader–Willi syndrome (PWS) is a neurodevelopmental disorder characterized by infantile hypotonia with reduced muscle tone, feeding difficulties, hypogonadism and hypogenitalism, hyperphagia and obesity, small hands and feet, mild mental deficiency, behavioral problems, and a characteristic face (small upturned nose, narrow bifrontal diameter, dolichocephaly.   Prader-Willi syndrome (PWS) is associated with an assortment of physical, behavioural and cognitive abnormalities which create a broad range of care needs. Information about the syndrome is spread across a variety of disciplines. In this book the authors seek to identify and provide the latest findings about how best to manage the complex medical, nutritional, psychological, educational.

    Prader-Willi syndrome (PWS) is a rare, genetic, multisystemic disorder, characterised by short stature, muscular hypotonia, intellectual disability, behavioural and psychological problems and frequently hypogonadism and impaired growth hormone secretion. PWS arises due to loss of function of paternally-expressed, imprinted genes from chromosome region 15qq In new-borns and infants, the. Prader–Willi syndrome (PWS) is a genetic disorder due to loss of function of specific genes. In newborns, symptoms include weak muscles, poor feeding, and slow development. Beginning in childhood, the person becomes constantly hungry, which often leads to obesity and type 2 diabetes. Also, mild to moderate intellectual impairment and behavioral problems are cations: Obesity, type 2 diabetes.


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Management of Prader-Willi Syndrome brings together the contributions of professionals with considerable expertise in diagnosis and management of PWS. Clinical, social, family, and community issues are explored and management strategies identified.

The text presents historical, medical, and genetic information to orient the reader.5/5(3). Management of Prader-Willi Syndrome brings together the contributions of professionals with considerable expertise in diagnosis and management of PWS. Clinical, social, family, and community issues are explored and management strategies identified.

The text presents historical, medical, and genetic information to orient the reader. Prader-Willi syndrome Weight Management Effective weight management is a crucial part of the care of a person with Prader-Willi syndrome (PWS) because obesity related complications are still the number one cause of death for people with PWS.

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 management.

It consists of contributions from professionals in many health and allied disciplines who have worked with this special : Springer New York. Helping All Families and Professionals, A Reference to PWSA (USA) Support and Services (Pamphlet). Management of Prader-Willi Syndrome brings together the contributions of professionals with considerable expertise in diagnosis and management of PWS.

Clinical, social, family, and community issues are explored and management strategies identified. The text presents historical, medical, and genetic information to orient the reader.

The major portion deals with pragmatic guidelines, rather than 5/5(1). Full Description: "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 management.

It consists of contributions from professionals in many health and allied disciplines who have worked with this special population.

The book focuses on clinical, social, familial, and community issues related to care. It is directed to health, education, and other specialists in academic, clinical, and community settings.

Management of Prader-Willi Syndrome describes strategies for management which. Management of Prader-Willi Syndrome brings together the contributions of professionals with considerable expertise in diagnosis and management of PWS.

Clinical, social, family, and community issues are explored and management strategies identified. The text presents historical, medical, and genetic information to orient the by: A Sleep Disorders in Prader-Willi Syndrome: Management Considerations / Gila Hertz and Mary Cataletto --App.

B Growth Charts for Prader-Willi Syndrome / Vanja A. Holm --App. C Food Exchange Guidelines --App. D Activity Therapy Guidelines --App. E.1 Weight Loss Treatment in an Institutionalized Individual with Prader-Willi Syndrome: A Case Study.

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 management. It consists of contributions from professionals in many health and allied disciplines who.

Get this from a library. Management of Prader-Willi syndrome. [Merlin Gene Butler; Phillip D K Lee; Barbara Y Whitman; Prader-Willi Syndrome Association.;] -- "Management of Prader-Willi Syndrome brings together the contributions of professionals with considerable expertise in diagnosis and management of PWS.

Clinical, social, family, and community issues. Management of Genetic Syndromes, Third Edition is a premier source to guide family physicians, pediatricians, internists, medical geneticists, and genetic counselors in the clinical evaluation and treatment of syndromes.

It is also the reference of choice for ancillary health professionals, educators, and families of affected individuals. Prader-Willi syndrome (PWS), the most common genetic cause of marked obesity in humans,17 is due to loss of expression of paternal genes from the 15qq13 region under the control of an.

Management of Prader-Willi Syndrome brings together the contributions of professionals with considerable expertise in diagnosis and management of PWS.

Clinical, social, family, and community issues are explored and management strategies identified. The text presents historical, medical, Price: $ Prader Willi syndrome (PWS) is a rare and complex genetic disease, with numerous implications on metabolic, endocrine, neurologic systems, with behavior and intellectual difficulties.

PWS is mainly characterized by severe hypotonia with feeding difficulties in the first years of life. Global developmental delays, hyperphagia with a gradual development of morbid obesity at about three years of : Maria A. Fermin Gutierrez, Magda D.

Mendez. Prader-Willi syndrome (PWS) is an uncommon genetic disorder characterized by mental retardation, decreased muscle tone, short stature, emotional lability and an insatiable appetite which can lead to life-threatening obesity.

The syndrome was first described in by Drs. Prader, Labhart, and Willi. from book Management of prader-willi syndrome: Third edition (pp) Prader-Willi syndrome (PWS) is characterized by hypotonia, obesity, hypogonadism, short stature, small hands and feet.

management of Prader-Willi syndrome throughout the life span to guide clinical practice. Participants: An open international multidisciplinary expert meeting was held in October in Toulouse, France, with 37 invited speakers and session chairs (see Acknowledgments) and 85 additional registered Size: 1MB.

A collection of true stories written by siblings who have a brother or sister with Prader-Willi syndrome. A book about siblings, for siblings. More suitable for older siblings / readers, it contains survey accounts which include details on the effects of having a sibling with PWS – the benefits, negatives, hardest parts and some advice for.

Management of Prader-Willi Syndrome by Merlin Butler,available at Book Depository with free delivery worldwide. Management of Prader-Willi Syndrome: Merlin Butler: We use cookies to give you the best possible experience.5/5(1).

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. Participants: An open international multidisciplinary expert meeting was held in October in Toulouse, France, with 37 invited speakers and session chairs (see Acknowledgments) and 85 additional registered Cited by:   Book Summary: The title of this book is Management of Prader-Willi Syndrome and it was written by Merlin Butler (Editor), Phillip D.K.

Lee (Editor), Barbara Y. Whitman (Editor). This particular edition is in a Hardcover format. This books publish date is and it has a suggested retail price of $Pages: