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Huntington's disease is a rare inherited neurological disorder that causes abnormal death of brain cells. Huntington is also known as HD and used to be known as Huntington's chorea. It affects about 1 in 10,000 people of Western European descent and 1 in 1,000,000 parents Africa and Asia. HD is a progressive disease This means that symptoms worsen with time.
HD is passed from one generation to another. If one parent has the mutated gene that causes Huntington's disease, their children will have a 50-50 chance of inheriting the gene. HD is usually hereditary, which means that it is hereditary, but in rare cases a person may develop disease without family history. This seems to be caused by a genetic mutation during development of sperm.
The symptoms of HD developed by usually later in the life of a person, but it is rare to happen early in life. If symptoms develop before the age of 20 years, it is known that the disease Juvenile Huntington's or juvenile HD.
Symptoms include uncontrollable movements known as chorea and balance problems and involuntary movements face. The difficulties with speech and swallowing problems may also occur. Depression and personality changes are other symptoms of HD, and advanced dementia.
Juvenile HD symptoms are often compared to Parkinson's disease. Muscle stiffness and rigidity can occur in adulthood, high definition, but are more common in patients under HD. Other symptoms include a decrease in juvenile HD academic performance, changes in handwriting, as well as problems of behavior and seizures.
HD symptoms worsen over time, to the point where patients need complete care afterward. Progression Juvenile HD is generally faster than adults in high definition.
Diagnose HD includes an in-depth history, both the patient's medical and the patient's family. Genetic blood tests can be done. For patients who are at risk of HD, but symptoms are not presented yet presymptomatic testing can be done to determine if they develop the disease at some point.
The treatments for HD can not slow down or stop its progression, but can help control and reduce complications. Some medications can help control involuntary movements and depression associated with the disease. Speech therapy can improve speech and swallowing help ensure adequate nutrition. Physiotherapy and exercise can help maintain muscle strength and combat depression.
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Huntington’s Disease Site, your source for information on Huntington’s disease symptoms, treatments and more.
Article Source: ArticlesBase.com – Huntington’s Disease Site
Flow – World’s End (HD)
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