Commonly Asked Questions Is there a special diet required for sufferers? The huntingtons DiseaseSociety of America (HDSA) is a national voluntary nonprofit organization http://endoflifecare.tripod.com/juvenilehuntingtonsdisease/id188.html
Extractions: Huntington's Disease (HD) also called Huntington's Chorea is an inherited disorder of the central nervous system. It causes progressive deterioration with varying symptoms which may include involuntary movements, speech impairment, and intellectual and emotional changes. Symptoms usually appear between the ages of 30 and 45, although they may appear earlier or later.
Download HDA Fact Sheets, Booklets & Forms Eating and swallowing difficulties 204k; Huntington s disease and diet Huntington s disease in the family (1997) - A booklet for young children http://www.hda.org.uk/charity/download.html
Extractions: The HDA Fact Sheets are available online in PDF format. To download, view and print out the HDA Fact Sheets you will require a copy of Adobe Acrobat Reader on your computer. Acrobat Reader is available for free and can be downloaded from the Adobe web site. You can also obtain printed copies of these fact sheets by contacting: All about the Huntington's Disease Association General information about Huntington's disease Predictive testing for Huntington's disease Talking to children about Huntington's disease ... Checklist for choosing a care home Membership Professional Membership Deed of Covenant Form with Bankers Order Huntington's disease in the family (1997) - A booklet for young children Facing Huntington's disease - A handbook for families and friends
What Is Huntington's Disease Huntington s disease, which is often called HD, is an hereditary disorder of A high calorie diet can prevent weight loss and improve symptoms such as http://www.hda.org.uk/charity/whatishd.html
Extractions: Huntington's disease, which is often called HD, is an hereditary disorder of the central nervous system. It used to be known as Huntington's Chorea or HC. Huntington's disease usually develops in adulthood and can cause a very wide range of symptoms. The disease affects both men and women. Huntington's disease is caused by a faulty gene on chromosome 4. The gene, which produces a protein called Huntingtin, was discovered in 1993. In some way - which is not yet understood - the faulty gene leads to a damage of the nerve cells in areas of the brain, including the the basal ganglia and cerebral cortex. This leads to gradual physical, mental and emotional changes.
HDA NORTH WEST LANCASHIRE BRANCH Huntington s disease is a dominantly inherited neurological disorder of thecentral nervous system. Huntington s disease and diet http://members.aol.com/hdanwlancs/
AllRefer Health - Huntington's Disease Prevention (Huntington Chorea) Huntington s disease (Huntington Chorea) information center covers Prevention . Since the odds that the child of a person with Huntington s disease will http://health.allrefer.com/health/huntingtons-disease-prevention.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 Alternate Names : Huntington Chorea Huntington's Disease Prevention Genetic counseling is advised if there is a family history of Huntington's disease. This may include DNA analysis of multiple family members. Since the odds that the child of a person with Huntington's disease will be affected are so high, people with the disorder may wish to consider adoption or forms of assisted reproduction that can reduce the chance that the disease will be passed on to their children.
Huntington's Disease Huntington s disease. By Karen Monte. Huntington s disease (HD) is a dominantgenetic disorder. Each child of a person who has HD has a 50% chance of http://www.lib.uchicago.edu/~rd13/hd/huntingtons.html
Extractions: Huntington's Disease (HD) is a dominant genetic disorder. Each child of a person who has HD has a 50% chance of inheriting the disease, and the disease does not skip a generation. HD is caused by a larger than normal CAG repeat in the Huntington gene. This larger than normal CAG repeat produces an abnormal protein that begins to kill brain cells when the person who has the gene reaches middle age. The loss of these cells causes intense symptoms and eventually death. HD was named after Dr. George Huntington. In 1872, he was the first person to document an accurate description of the symptoms and course of the disease. At the time he called it hereditary chorea. The Huntington gene was discovered in 1993 by the Huntington Study Group. The CAG repeats in the Huntington gene, which is located on chromosome 4, code for the protein huntingtin. The larger than normal number of CAGs in a person with HD causes the huntingtin protein to be abnormal, which leads to symptoms. Even though every cell in the body has the gene, only the cells in the brain seem to be affected. A person has two alleles for every gene. One allele is inherited from the mother and one allele is inherited from the father. If either allele of the Huntington gene has the larger than normal CAG repeat, the person will have HD. If neither allele has the larger than normal CAG repeat, the person will not have HD and will not pass it on. When a person has children, only one allele of each gene is passed on. If a person with HD passes on the allele with the larger than normal CAG repeat, the child will have HD. If the allele with the normal CAG is passed on, the child will not have HD.
NINDS Forwarding Page Today, physicians commonly use the simple term Huntington s disease (HD) to The individual s physician can offer additional advice about diet and about http://www.ninds.nih.gov/health_and_medical/pubs/huntington_disease-htr.htm
Extractions: NINDS has redesigned its website and the URL for the page you were seeking has changed. The new URL for this page is /disorders/huntington/detail_huntington.htm . Please update your bookmark to this page. You will be automatically taken to this page in 5 seconds, or you can click the link to go there now.
Huntington's Disease Association Of Ireland The Huntington s disease Association of Ireland (HDAI) provides consultation,information and individualised support to those diagnosed with Huntington s http://www.huntingtons.ie/question.html
Extractions: Huntingtons Disease (HD) also called Huntingtons Chorea is an inherited disorder of the central nervous system. It causes progressive deterioration with varying symptoms which may include involuntary movements, speech impairment, and intellectual and emotional changes. Symptoms usually appear between the ages of 30 and 45, although they may appear earlier or later. How does the disease get its name? This is a genetic disease. Each child of an affected parent has a one in two chance or 50% likelihood of inheriting the gene. People with the abnormal gene will always develop the disease, unless they die of other causes prior to developing signs and symptoms.. People who do not inherit the HD gene will not develop the disease, neither will their children, or the childrens children. The disease does not skip a generation. How is it caused?
Testing For Huntington's Disease - Part One This is an article on testing for Huntington s disease. The information in thisarticle comes from the booklet entitled, Testing for Huntington s disease http://www.suite101.com/article.cfm/huntingtons/30924
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Reader Survey messages from 1 to 1 of Discussions relating to Huntington s disease ReaderSurvey - dewey decimal 616.851. http://www.suite101.com/discussion.cfm/huntingtons/29023
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$500,000,000 Market For Huntingtons' Disease Treatment Huntington s disease Fast track approval ofLAX101 for the treatment ofHuntington s disease. Market for LAX-100 estimated at $500000000. http://hdlighthouse.org/treatment-care/treatment/drugs/lax101/human/updates/0034
Extractions: "When you cut through all the detail, this could be a drug that is very significant for the treatment of Huntington's", Rick Stewart, Amarin CEO Amarin Corp is a $25 million British company that licenses and sells drugs to treat nerve disorders, like Parkinson's Disease. Amarin's chief executive, Rick Stewart, hails from SkyePharma a British drug developer. Stewart says that Amarin's research partner, Laxdale of Scotland, will follow up any day now on preliminary findings from a Phase III study of LAX-101, a treatment for Huntington's Disease. "This is the first time we have seen anything positive for Huntington's," says Stewart, who is shaking his head about the market's treatment of the preliminary findings. A study of 83 qualifying patients took place at Harvard, Emory and Johns Hopkins universities, and in the United Kingdom and Canada. Huntington's, a genetic disorder, has been diagnosed in about 30,000 Americans and an equal number of patients in Europe. The U.S. Food and Drug Administration has granted LAX-101 a so-called fast-track designation.
Extractions: Huntington's Disease D ominant and Faulty Genetic Disorder Hereditary Chorea " LEARN MORE, BE MORE " Last-Modified: Foogle Business - Huntington's Disease - Huntingtons - Huntingdons Learn More, Be More What is Huntington's Disease What is Huntington's Disease? It is due to a dominant and faulty genetic disorder on chromosome 4 The consequence of the fault with this gene starts around or just before middle age, and leads to a gradual physical, mental and emotional change in its victim. Huntington's Disease was named after the American, Dr. George Huntington, because in 1872 he was the first person to document an accurate description of the symptoms and the route of the disease. The cause was then unknown. Huntington's Disease - Hereditary Chorea George Huntington (1850-1916) George Huntington was born on 9 April 1850 in the drowsy secluded village of East Hampton, CT, United States. Both his father and grandfather were doctors, and George Huntington junior followed in their footsteps. At an early age, Huntington accompanied his father on his rounds and sick calls and during one of these visits, he gained his first experience of hereditary chorea. At the time he called it Hereditary Chorea.
Huntington's Disease - Treatment - Neurologychannel There is no cure for huntingtons disease. Treatment focuses on addressing thedisease s symptoms, preventing associated complications and providing support http://www.neurologychannel.com/huntingtons/treatment.shtml
Untitled Document First we will look at what genetic changes give rise to genetic diseases, huntingtons s disease has a test, which can be performed on a fetus. http://www.stanford.edu/class/bio4/ClassLinks/october11.htm
Extractions: http://www.kumc.edu/gec/support/ We all want our children to be better off than we are. We hope they will be better educated, healthier, financially more secure. 5-10% of children inherit and identifiable genetic defect. Some more serious than others i.e. asthma to sickle cell anemia. Till now medicine has largely been about treating the symptoms but now the hope or promise of Biotechnology is that embryos can be prescreened for disease and even diseases that have childhood or adult onset can be treated. First we will look at what genetic changes give rise to genetic diseases, and what are some examples of these diseases. Second we will look at how biotechnology might treat various genetic diseases. Genetic mutations can take the form of the loss or addition of a single of a few bases or large loss or rearrangement of chromosome pieces or abnormal numbers of whole chromosomes. Genetic Disease Alteration in chromosome structure Inversions
Extractions: highest quality supplements at the lowest cost in the industry. Enhanced Life Sciences products are recommended by physicians and nurses for individuals with Parkinson's disease, ALS, MS, CHF, HIV/AIDS and many other disorders. Enhanced Life Sciences offers all of our customer's access to our on-staff Registered Dietitian
Extractions: path = "http://www.enhancedlifesciences.com/"; Home About Us Products Disorders ... Cart Muscular Dystrophy Association - The Muscular Dystrophy Association is a voluntary health agency a dedicated partnership between scientists and concerned citizens aimed at conquering neuromuscular diseases that affect more than a million Americans. Neuromuscular Disease Center - Clinical services for neuromuscular disorders as well as the regional MDA Clinic. Strength-L - An internet discussion list dedicated to people who have a form of neuromuscular disease . Information about the group, subscribing instructions and browse the archives. Lincolnshire Post-Polio Library: Neuromuscular Junction Transmission Defects - Article about anticholinesterase-responsive neuromuscular junction transmission defects in post-poliomyelitis fatigue. Neuromuscular Disease Center - Review of various muscle, nerve and neuromuscular disorders; links to relevant sites. Neuromuscular Junction Effects - Description of acetylcholinesterase inhibitors producing destructive changes at the neuromuscular junction. For medical professionals. Disorders of the Neuromuscular Junction - An introduction to disorders of the neuromuscular junction from Baylor College of Medicine.
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Antibiotic Holds Promise As Huntington's Treatment To learn more about Huntington s disease, visit the huntingtons disease Societyof America (www.hdsa.org ). SOURCES Stephen Massa, MD, Ph.D., http://ww3.komotv.com/Global/story.asp?S=3688405
Huntington Disease Table 1. Molecular Genetic Testing Used in Huntington disease Supportive carewith attention to nursing, diet, special equipment, and eligibility for http://www.geneclinics.org/profiles/huntington/details.html
Extractions: 30 August 2005 Disease characteristics. Huntington disease (HD) is a progressive disorder of motor, cognitive, and psychiatric disturbances. The mean age of onset is 35 to 44 years and the median survival time is 15 to 18 years after onset. Diagnosis/testing. The diagnosis of HD rests on positive family history , characteristic clinical findings, and the detection of an expansion in the HD gene that is 36 or more CAG trinucleotide repeats Genetic counseling HD is inherited in an autosomal dominant manner. Offspring of an individual with a mutant allele have a 50% chance of inheriting the disease-causing allele Predictive testing in asymptomatic adults at 50% risk is available, but requires careful thought, including pretest and post-test genetic counseling , as no treatment exists. Asymptomatic at-risk individuals younger than 18 years of age should not have predictive testing . Although infrequently requested
