AllRefer Health - Huntington's Disease (Huntington Chorea) Huntington s disease. Definition. Huntington s disease is an inherited conditioncharacterized by abnormal body movements, dementia, and psychiatric problems. http://health.allrefer.com/health/huntingtons-disease-info.html
Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Go To Main Page Alternate Names : Huntington Chorea Definition Huntington's disease is an inherited condition characterized by abnormal body movements, dementia , and psychiatric problems. Huntington's disease is a progressive disorder involving wasting (degeneration) of nerve cells in the brain. The disorder was first described in 1872 by George Huntington, an American physician. Huntington's disease is inherited as a single faulty gene on chromosome #4. There is a part of the gene that is repeated in multiple copies. The greater the number of repeats, the more likely it is that the person will develop symptoms and the greater the chance they will occur at a younger age. The disease may occur earlier and more severely in each succeeding affected generation because the number of repeats can increase. Every child of a parent with the disorder has a 50% chance of inheriting Huntington's Disease. Symptoms do not usually appear until adulthood, typically between ages 35 and 50 years old but this depends on the number of repeats found in the gene so it may also appear in younger people. In children it may appear to be Parkinson's disease with rigidity, slow movements, and tremor.
AllRefer Health - Huntington's Disease Treatment (Huntington Chorea) Huntington s disease. Huntington s disease Treatment. There is no cure for Huntington sdisease, and there is no known way to stop progression of the disorder. http://health.allrefer.com/health/huntingtons-disease-treatment.html
Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Medications vary depending on the symptoms. Dopamine blockers such as haloperidol or phenothiazine medications may reduce abnormal behaviors and movements. Reserpine and other medications have been used, with varying success. Drugs like Tetrabenazine and Amantadine are used to try to control extra movements. There has been some evidence to suggest that Co-Enzyme Q10 may minimally decrease progression of the disease.
Resources For Daily Living With Huntington's Disease Available from Huntington s disease Society of America, 158 West 29th Street, 7thFloor instant food thickener, instant pasta for the purée diet, heat and http://www.lib.uchicago.edu/~rd13/hd/daily.html
Extractions: Compiled by Renette Davis with assistance from people on the Mailing List for Huntington's Disease Company that makes the merriwalker, latest version of which is "untippable." Used by one member of the Mailing List for Huntington's Disease for someone with juvenile HD who cannot stand up or walk on his own. Address: P.O. Box 374, Talmadge, Ohio, 44278. Phone: 1-800-628-1441. Cost of the merriwalker is about $280.00. Company which makes a wheelchair that is padded. Some people on the Mailing List for Huntington's Disease report that it is difficult to push, but it seems to be very comfortable for people with Huntington's Disease and it was paid for by Medicare. Address: 72 Victoria Street South, Kitchener, Ontario N2G 2A9 Canada. Phone: 519-578-9630 or 800-225-5288. Wonderful web site from Dr. Richard Dubinsky at the Kansas University Medical Center. Includes articles on communication strategies, eating and swallowing, genetics of HD, home safety, etc. Available at: http://www.kumc.edu/hospital/huntingtons/index.html
HD Information disease 47k; Information for Teenagers - 41k; Eating and SwallowingDifficulties - 104k; Huntington s disease and diet - 120k; The http://endoflifecare.tripod.com/kidsyoungadults/id6.html
Extractions: The patient with moderate Huntington's disease, like any person suffering from a chronic disease, can become an easy target for abuse. This can be a result of the mental changes that he or she has undergone, the caregivers inability to adapt fast enough, or the fact that the patient with Huntington's disease is an easily identified victim. The abuse can be either way. A caregiver can abuse the patient and the patient can abuse the caregiver and the rest of the family. The section on behavior has information on working with the behavioral changes associated with Huntington's disease. A practical guide for individuals, families and professionals coping with HD Jane S. Paulsen, PhD, 2000. A must-read for anyone who deals extensively with an HD-affected individual; ex plains not only the behavior challenges created by HD, but their origin in the HD-affected brain. By understanding the basis of these behaviors, Dr. Paulsen is able to suggest effective ways of dealing with and preparing for them. The book also covers environmental, individual and health factors that contribute to behavior problems. Problem-solving tips and techniques are given for behaviors arising from communication difficulties, memory problems, cognitive break
Testing For Huntington's Disease - Part One - Suite101.com since currently there is no medical benefit (for example, early treatment, specificdiet, or lifestyle changes), that can slow or prevent Huntington s disease. http://www.suite101.com/article.cfm/huntingtons/30924
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DentalCareNews0903 Firstly, the person with Huntingtons disease usually lacks the dexterity to usea toothbrush efficiently, if at all. Secondly, the diet of the person tends http://homepages.ihug.co.nz/~ghtaylor/DentalCare.htm
Extractions: Graham Taylor Site Resources available from the Homepage Articles taken from the Sept. 2003 Huntington's News. The Quarterly Newsletter of the Huntington's Disease Associations of New Zealand The Importance of Dental Care in Huntington Disease It should be stated at the outset that the teeth of people with Huntington Disease (HD) are no different from those of other people. They are not innately more susceptible to tooth decay or gum disease, but people with HD do present clinically with more dental problems. For the dentist, treatment of patients with advanced Huntington Disease is difficult. The dentist can be faced with a patient who, needing a number of fillings, cannot open his mouth widely, or cannot sit still, or both. Possible financial difficulties, transport problems, access to dental surgeries, and apathy or resentment in the patient and/or family, all contribute to the fact that treatment is frequently neglected. It is possible that a person with such rampant decay would often be advised to have all teeth removed and full dentures constructed; but for the person with HD this can be the beginning of more problems. Initially a full denture stays in by suction, but more important is the pull of the facial muscles forcing the dentures into place. This muscle activity is automatic, but in HD, such low-level muscle activity is often overridden by uncontrolled involuntary movements that can frequently and spontaneously eject the denture from the mouth. Eating for people experiencing this can be a real trial, further aggravating their dysphagia (difficulty swallowing). For the person with no teeth and no denture an attractive facial appearance is destroyed by loss of cheek and lip support. Consequently, there is a lowering of self-esteem apart from the lack of function.
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New Page 1 The momentum in Huntington s disease research continues to accelerate and qualityof life for people with the disease. of the importance of diet and general http://www.hdasa.org.au/hdfacts.htm
Extractions: Often personality changes accompany the muscle movements. Many people with Huntington's Disease become sad and moody, others apathetic and unmotivated. Sometimes little things may upset them and their tempers are very short. They easily become angry and are sometimes very suspicious of others. Occasionally, a person may seem very happy and carefree.
Health Subject Help Diabetes, diet therapy recipes, 641.56314. the quarterly newsletter of the Huntington sDisease Association of Official website is at www.huntingtons.org.nz. http://www.wcl.govt.nz/pathfinders/health.html
Extractions: Home Subject Help Health Subject Help Quicksearch for major medical conditions Shelf numbers Electronic resources Magazines ... Vertical file This pathfinder is designed for you to easily access the wealth of Health resources available in the Wellington City Libraries. It does not include links to online health sites, except those that the library subscribes to. If you are reading this at an OPAC, you will not be able to access these online sites, however you can access them at any enquiries desk, or from elsewhere if you have a valid password on your Wellington City Libraries card. Health information from the library should not be regarded as professional advice from a qualified doctor or health professional. This information is not designed to replace the advice and care that can be obtained from a health professional. Wellington City Libraries provides health information to enable better communication between health professionals and their patients. The library will not offer advice on medical and health issues. Clicking on any of these topics will bring up 'subjects'. To bring up individual items, click on the subject heading that is closest to what you need.
Genetics Primer Huntington disease. Example individual who inherits a combination of alleles whichmakes them susceptible to coronary heart disease if their diet is high http://www.bmb.psu.edu/faculty/simpson/lab/03geneti/03geneti.htm
CheatHouse.com - Huntingtons Disease If you need help browsing, viewing or submitting (350 points) essays, click here.huntingtons disease. huntingtons disease. CheatHouse. Februar 13, 2003. http://www.cheathouse.com/essay/essay_view.php/p_essay_id/12081
Extractions: (chat history) If you need help browsing, viewing or submitting (350 points) essays, click here. Subject: Click here to submit a new essay to this category Author: Date: Februar 13, 2003 Level: College, 2nd, Sophomore Change Grade: Change Size (words): Essay Status: regular No of views: Essay rating: (total score: 8) View as: Original or Line Formatted Download: In "Genetics and Reproductive Risk: Can having children be immoral," L.M Purdy discusses the notion that the recent advances in reproductive technology impose a moral obligation on individuals to prevent the birth of "affected" babies that will not have a "minimally satisfying life." There are, however, several assumptions that the author makes in reaching the conclusion that having "affected" children ... Showed first 50 words of 858 Size (words) ...
Untitled Document How Quickly Does diet Make for Change ? 223 E Cheraskin DMD, MD. Control ofHuntingtons disease by Orthomolecular Treatment 229 A Hoffer, MD, PhD. http://www.orthomed.org/jom/jom87.htm
Diseases & Disorders CARING FOR PEOPLE WITH HUNTINGTON S disease http//www.kumc.edu/hospital/huntingtons/This page provides information for those with Huntington s disease, those http://www.kckpl.lib.ks.us/refdept/cnhealth/Disease.htm
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