21st Century Huntington's Disease (HD) Sourcebook: Clinical Data for Patients, Families, and Physicians - Hereditary Chorea, Diagnosis, Symptoms, Genetics, Medications, Clinical Trials

Nonfiction, Health & Well Being, Health, Ailments & Diseases, Genetic, Nervous System & the Brain
Cover of the book 21st Century Huntington's Disease (HD) Sourcebook: Clinical Data for Patients, Families, and Physicians - Hereditary Chorea, Diagnosis, Symptoms, Genetics, Medications, Clinical Trials by Progressive Management, Progressive Management
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Author: Progressive Management ISBN: 9781301823178
Publisher: Progressive Management Publication: November 21, 2012
Imprint: Smashwords Edition Language: English
Author: Progressive Management
ISBN: 9781301823178
Publisher: Progressive Management
Publication: November 21, 2012
Imprint: Smashwords Edition
Language: English

This comprehensive ebook provides authoritative information and practical advice from the nation's health experts about Huntington's Disease, also known as hereditary chorea. Starting with the basics, and advancing to detailed patient-oriented and physician-quality information, the 21st Century Sourcebook series gives empowered patients, families, caregivers, nurses, and physicians the information they need to understand this disease. There is coverage of symptoms, diagnosis, medical testing, clinical research, drugs and potential treatments.

HD results from genetically programmed degeneration of nerve cells, called neurons, in certain areas of the brain. This degeneration causes uncontrolled movements, loss of intellectual faculties, and emotional disturbance. Specifically affected are cells of the basal ganglia, structures deep within the brain that have many important functions, including coordinating movement. Within the basal ganglia, HD especially targets neurons of the striatum, particularly those in the caudate nuclei and the pallidum. Also affected is the brain's outer surface, or cortex, which controls thought, perception, and memory. HD is found in every country of the world. It is a familial disease, passed from parent to child through a mutation or misspelling in the normal gene. The rate of disease progression and the age at onset vary from person to person. Adult-onset HD, with its disabling, uncontrolled movements, most often begins in middle age. There are, however, other variations of HD distinguished not just by age at onset but by a distinct array of symptoms. For example, some persons develop the disease as adults, but without chorea. They may appear rigid and move very little, or not at all, a condition called akinesia.

Contents: Chapter 1: National Institute of Neurological Disorders and Stroke (NINDS) Information * Chapter 2: National Human Genome Research Institute (NHGRI) Information * Chapter 3: Centers for Disease Control and Prevention (CDC) Information * Chapter 4: FDA Information * Chapter 5: National Institutes of Health Research Portfolio Online Reporting Tools (RePORT) Studies * Chapter 6: Clinical Trials * SECTION B: GUIDE TO LEADING MEDICAL WEBSITES; INTERNET RESOURCES FOR MEDICAL AND HEALTH INFORMATION

This edition includes our exclusive Guide to Leading Medical Websites with updated links to 81 of the best sites for medical information, which let you quickly check for updates from the government and the best commercial portals, news sites, reference/textbook/non-commercial portals, and health organizations.

View on Amazon View on AbeBooks View on Kobo View on B.Depository View on eBay View on Walmart

This comprehensive ebook provides authoritative information and practical advice from the nation's health experts about Huntington's Disease, also known as hereditary chorea. Starting with the basics, and advancing to detailed patient-oriented and physician-quality information, the 21st Century Sourcebook series gives empowered patients, families, caregivers, nurses, and physicians the information they need to understand this disease. There is coverage of symptoms, diagnosis, medical testing, clinical research, drugs and potential treatments.

HD results from genetically programmed degeneration of nerve cells, called neurons, in certain areas of the brain. This degeneration causes uncontrolled movements, loss of intellectual faculties, and emotional disturbance. Specifically affected are cells of the basal ganglia, structures deep within the brain that have many important functions, including coordinating movement. Within the basal ganglia, HD especially targets neurons of the striatum, particularly those in the caudate nuclei and the pallidum. Also affected is the brain's outer surface, or cortex, which controls thought, perception, and memory. HD is found in every country of the world. It is a familial disease, passed from parent to child through a mutation or misspelling in the normal gene. The rate of disease progression and the age at onset vary from person to person. Adult-onset HD, with its disabling, uncontrolled movements, most often begins in middle age. There are, however, other variations of HD distinguished not just by age at onset but by a distinct array of symptoms. For example, some persons develop the disease as adults, but without chorea. They may appear rigid and move very little, or not at all, a condition called akinesia.

Contents: Chapter 1: National Institute of Neurological Disorders and Stroke (NINDS) Information * Chapter 2: National Human Genome Research Institute (NHGRI) Information * Chapter 3: Centers for Disease Control and Prevention (CDC) Information * Chapter 4: FDA Information * Chapter 5: National Institutes of Health Research Portfolio Online Reporting Tools (RePORT) Studies * Chapter 6: Clinical Trials * SECTION B: GUIDE TO LEADING MEDICAL WEBSITES; INTERNET RESOURCES FOR MEDICAL AND HEALTH INFORMATION

This edition includes our exclusive Guide to Leading Medical Websites with updated links to 81 of the best sites for medical information, which let you quickly check for updates from the government and the best commercial portals, news sites, reference/textbook/non-commercial portals, and health organizations.

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