The Huntington’s Disease

The Huntington’s Disease

The Huntington’s Disease

The Huntington’s Disease:Huntington’s disease is a genetic disorder that affects the coordination of muscles and as a consequence, there is a cognitive failure and behavioral symptoms. The disease can affect both genders, and it becomes noticeable during the early years of adulthood. Autosomal dominant mutation takes place between two gene replicas referred to as Huntingtin. In this case, therefore, it means that a child born to parents with such condition is likely to inherit the disease. The fact that its symptoms become noticeable between the ages of thirty years to forty years doesn’t mean that the illness cannot develop earlier. There are certain cases when the disease can develop in a child. In cases where the disorders begin to be recognized at in teenage years, the condition is referred to as juvenile Huntington’s disease.

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Huntington’s disease cases were reported many years ago, and researchers have been trying to develop a cure for the disease. But major achievements have been on how to mitigate the effects of Huntington’s disease. The researchers have performed experiments on animals such as mice for the purpose of finding out how HD protein can be controlled. It also shows that the disease can affect both adults and young people, and the difference is seen in the symptoms.

References
Shoulson, I., & Fahn, S. (1979). Huntington disease clinical care and evaluation. Neurology, 29(1), 1-51.

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