Wilson Disease

Nonfiction, Health & Well Being, Medical, Specialties, Internal Medicine, Neurology
Cover of the book Wilson Disease by , Elsevier Science
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Author: ISBN: 9780444636270
Publisher: Elsevier Science Publication: April 18, 2017
Imprint: Elsevier Language: English
Author:
ISBN: 9780444636270
Publisher: Elsevier Science
Publication: April 18, 2017
Imprint: Elsevier
Language: English

Wilson Disease provides a comprehensive guide on this inherited genetic disorder that has devastating consequences for both the liver and neurologic/psychiatric health. This disease is of increasing interest to neurologists, hepatologists, and geneticists, but when the disease is diagnosed early, it is treatable, with patients living normal lives.

This volume describes the molecular pathophysiology of WD and the clinical and pathological effects of copper. Separate sections address both diagnosis and medical and surgical approaches to treatment. Both adult and pediatric perspectives on diagnosis and treatment are addressed, and a section on genetics highlights advances in molecular diagnostics. Patient support groups that can aid in coping with this disease are also discussed, as are animal models for those interested in basic research on cell biology, pathophysiology, and treatment.

  • Addresses the molecular pathophysiology of WD and the clinical and pathological effects of copper
  • Offers coverage of both diagnosis and medical and surgical approaches to treatment
  • Includes perspectives on both adult and pediatric diagnosis and treatment
  • Edited work with chapters authored by leaders in the field from around the globe—the broadest, most expert coverage available
View on Amazon View on AbeBooks View on Kobo View on B.Depository View on eBay View on Walmart

Wilson Disease provides a comprehensive guide on this inherited genetic disorder that has devastating consequences for both the liver and neurologic/psychiatric health. This disease is of increasing interest to neurologists, hepatologists, and geneticists, but when the disease is diagnosed early, it is treatable, with patients living normal lives.

This volume describes the molecular pathophysiology of WD and the clinical and pathological effects of copper. Separate sections address both diagnosis and medical and surgical approaches to treatment. Both adult and pediatric perspectives on diagnosis and treatment are addressed, and a section on genetics highlights advances in molecular diagnostics. Patient support groups that can aid in coping with this disease are also discussed, as are animal models for those interested in basic research on cell biology, pathophysiology, and treatment.

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