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Management of Prader-Willi Syndrome

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  • © 2022
  • Latest edition

Overview

  • The most comprehensive resource on Prader-Willi Syndrome (PWS) available, in a fully revised 4th edition
  • Divided into sections on genetics and diagnosis, physiology and treatment, and multidisciplinary management
  • Growth charts, benefits eligibility information and additional resources are included in helpful appendices

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Table of contents (26 chapters)

  1. Diagnosis, Clinical Aspects and Genetics of Prader-Willi Syndrome

  2. Medical Physiology and Treatment

  3. Multidisciplinary Management of Prader-Willi Syndrome

Keywords

About this book

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 significant changes in the diagnosis, clinical care and treatment of PWS since the previous edition was published in 2006, and more thorough information on understanding the cause and diagnosis of the condition, along with clinical presentation and findings with natural history data now available. 


The book is divided into three thematic sections. Part One discusses the genetics, diagnosis, research and overview of PWS, including current laboratory testing. The medical physiology and treatment of PWS comprise Part Two, covering the GI system, obesity as well as the use of growth hormone. Part Three, the largest section, presents a wide-ranging, multidisciplinary management approach to PWS, attending to the many manifestations of the condition. Topics here include neurodevelopmental aspects, speech and language disorders, motor issues, psychological and behavioral management, educational and transitional considerations, vocational training and residential care, and advocacy for both school discipline and sexuality. Syndrome-specific growth charts, benefits eligibility information and additional resources are included in helpful appendices. 


Timely and well-crafted, this latest edition of Management of Prader-Willi Syndrome remains the gold standard for clinicians and health care providers working with patients diagnosed with this rare obesity-related genetic disorder.


Editors and Affiliations

  • Departments of Psychiatry & Behavioral Sciences and Pediatrics, University of Kansas Medical Center, Kansas City, USA

    Merlin G. Butler

  • Department of Pediatrics, University of Texas Medical Branch, Galveston, USA

    Phillip D. K. Lee

  • Department of Pediatrics, Saint Louis University, St. Louis, USA

    Barbara Y. Whitman

About the editors

Merlin G. Butler, MD, PhD, Director, Division of Research and Genetics, Director, KUMC Genetics Clinic, Departments of Psychiatry & Behavioral Sciences and Pediatrics, University of Kansas Medical Center, Kansas City, KS, USA


Phillip D. K. Lee, MD, Department of Pediatrics, University of Texas Medical Branch, Galveston, TX, USA


Barbara Y. Whitman, PhD, Department of Pediatrics, Saint Louis University, Saint Louis, MO, USA

Bibliographic Information

  • Book Title: Management of Prader-Willi Syndrome

  • Editors: Merlin G. Butler, Phillip D. K. Lee, Barbara Y. Whitman

  • DOI: https://doi.org/10.1007/978-3-030-98171-6

  • Publisher: Springer Cham

  • eBook Packages: Medicine, Medicine (R0)

  • Copyright Information: The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG 2022

  • Hardcover ISBN: 978-3-030-98170-9Published: 11 October 2022

  • Softcover ISBN: 978-3-030-98173-0Published: 11 October 2023

  • eBook ISBN: 978-3-030-98171-6Published: 10 October 2022

  • Edition Number: 4

  • Number of Pages: X, 541

  • Number of Illustrations: 25 b/w illustrations, 53 illustrations in colour

  • Topics: Endocrinology, Pediatrics, Psychiatry

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