Huntingtons Disease by Oliver W J QuarrellHuntingtons Disease by Oliver W J Quarrell

Huntingtons Disease

byOliver W J Quarrell

Paperback | March 15, 2008

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Huntington's disease is a genetically inherited condition which results in severe nerve-cell damage in the brain. The hereditary and debilitative nature of the disease means that many people are involved either directly or indirectly by this condition. The recent identification of the faultygene involved has made the diagnosis of this condition simpler. The majority of people develop the disease between the ages of 35 and 55 years, so for those aware of their genetic risk there are dilemmas to consider - should you have a test to see if you have the gene? Should you start a family?The new edition of this successful book specifically designed for families of patients with Huntington's disease has been expanded to include a number of important new developments in research and clinical practice that have occurred in the field in recent years. While there are no drugs currentlyavailable that slow down or reverse the neurodegenerative process in Huntington's Disease, there is growing data on the use of existing treatments to manage movement disorder, irritability and depression associated with the condition, which are covered here. This edition also includes completely newchapters covering juvenile Huntington's disease and late-stage Huntington's disease, and a fully updated Appendix of relevant patients' organizations.
Dr Oliver Quarrell has been elected to the Executive Council of the Huntington's Disease Association and currently serves as its vice Chairman. He is also actively involved in the European Huntington's Disease Network.
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Title:Huntingtons DiseaseFormat:PaperbackDimensions:176 pages, 7.72 × 5.08 × 0.38 inPublished:March 15, 2008Publisher:Oxford University PressLanguage:English

The following ISBNs are associated with this title:

ISBN - 10:0199212015

ISBN - 13:9780199212019

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Table of Contents

1. Facts and figures about Huntington's disease2. The physical features of Huntington's disease3. Behavioural and emotional aspects of Huntington's disease4. Juvenile Huntington's disease5. The genetics of Huntington's disease6. Laboratory test results7. Genetic counselling: a new diagnosis in the family8. Genetic counselling for unaffected family members9. Changes in the brain10. What causes selective nerve cell damage?11. Current research activities12. Useful resources and contacts