much about Huntington’s disease. After reading this paper and the subsequent ones to come‚ you surely will. According to PudMedHealth.com‚ “Huntington’s disease is a disorder passed down through families in which nerve cells in certain parts of the brain waste away or degenerate.” This can lead to many different complications to a person’s health. In most cases‚ the disease’s symptoms develop later in life during a person’s mid thirties-forties. There are also instances where the disease becomes on-set
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Huntington’s Disease Huntington’s disease‚ also known as Huntington’s chorea is a genetic disorder that usually shows up in someone in their thirties and forties‚ destroys the mind and body and leads to insanity and death within ten to twenty years. The disease works by degenerating the ganglia (a pair of nerve clusters deep in the brain that controls movement‚ thought‚ perception‚ and memory) and cortex by using energy incorrectly. The brain will starve the neurons (brain cells)‚ and sometimes
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Huntington’s Disease Definition- Huntington’s Disease is an inherited disease that causes the progressive breakdown of nerve cells in the brain. Classification- This disease affects the musculoskeletal system due to loss of brain cells that control the initiation‚ coordination and fluidity of movement. This disease also affects the digestive system due to the loss of muscle control affects chewing and swallowing. The American Speech-Language-Hearing Association notes that people with Huntington
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Huntington’s Disease Background Huntington’s disease is inherited as an autosomal dominant disease that gives rise to progressive‚ elective (localized) neural cell death associated with choleric movements (uncontrollable movements of the arms‚ legs‚ and face) and dementia. It is one of the more common inherited brain disorders. About 25‚000 Americans have it and another 60‚000 or so will carry the defective gene and will develop the disorder as they age. Physical deterioration occurs over a period
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Huntington’s Disease Huntington’s Disease (HD) is a hereditary neurological disorder of the central nervous system that causes progressive degeneration of cells in the brain. This degeneration causes the affected person to slowly loose the ability to move‚ communicate and think. People are born with this disease‚ but won’t develop symptoms until between the ages of 30 – 50. Although Huntington’s disease can be traced back to the Middle Ages‚ it was first described by American physician George
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Huntington ’s disease John Doe HCS/245 10/20/2013 Prof Jane Huntington ’s disease In 1993 researchers discovered the gene that causes Huntington’s disease. (Huntington ’s disease Society of America‚ 8/27) Huntington’s disease is a disease which progressively degenerates cells in the brain slowly over time. Since the nerve cells in the brain are slowly dying it causes uncontrollable movements‚ emotion changes and other forms of determination of psychological aspects. (The Diagnosis and
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Huntington’s Disease Garry Estrada University of Phoenix PSYCH/575 February 6‚ 2011 Rex Philpot‚ Ph.D. Huntington’s Disease The human body in its ability to function properly is comprised of the central nervous system‚ the peripheral nervous system‚ and the autonomic nervous system‚ which is a “branch of the peripheral nervous system” (Carlson‚ 2010‚ p. 97). The central nervous system and the peripheral nervous system make up the primary controls that command all
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Abstract This paper sheds light on one of the most important diseases which is Huntington’s disease (HD). It’s widely spread around the world but it’s not commonly known among people. Since science developed and genetics became known‚ scientists discovered that HD is inherited from one generation to another which have put the scientists with a big challenge to find cure for such disease. In addition‚ this paper provides information about causes‚ symptoms‚ inheritance‚ treatments
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Huntington’s Disease is a homozygous dominant neurodegenerative disorder caused by a mutation in the HD gene. The mutation involves the basal ganglia‚ striatum and cerebral cortex parts of the brain and causes a CAG trinucleotide repetition. This repetition then proceeds to cause involuntary chorea‚ mood disorders‚ mental instability‚ and eventually leads to death. Since this is a relatively new discovery the Huntingtin gene is still mysterious in many ways to researchers. Many new discoveries have
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Huntington’s disease is an inherited disease. Huntington disease results from altered activity of basal nuclei neurons. Basal nuclei neurons gradually deteriorate‚ resulting in unrestrained movement. Huntington’s disease has a extreme impact on a person’s functional abilities and usually results in movement‚ thinking and psychiatric disorders. Most people with Huntington’s disease will develop signs and symptoms in their 30s or 40s. But the disease can emerge earlier or later in life. If the disease
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