33: Huntington's Disease Brain Vs Normal Brain

Huntingtons disease is a rare neuropsychiatric disorder with a prevalence of 5 10 per 100000 in the caucasian population. Huntingtons disease is a condition that stops parts of the brain working properly over time.

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Huntingtons disease hd also known as huntingtons chorea is a neurodegenerative disease that is mostly inherited.

Huntingtons disease brain. The onset of the disease is usually in adulthood with a life expectancy of about 10 to 30 years. It is also a basal ganglia disease causing a hyperkinetic movement disorder known as chorea. As the disease advances uncoordinated.

Symptoms of the disease which gets progressively worse include uncontrolled movements called chorea abnormal body postures and changes in. Huntingtons disease hd is an inherited neurological illness causing involuntary movements severe emotional disturbance and cognitive decline. Its passed on inherited from a persons parents.

History and genetics of huntingtons disease. Huntingtons disease is a degenerative neurological condition affecting the nerve cells in the brain. Huntingtons disease hd is an inherited disorder that causes brain cells called neurons to die in various areas of the brain including those that help to control voluntary intentional movement.

This defect is dominant meaning that anyone who inherits it from a parent with huntingtons will eventually develop the disease. The earliest symptoms are often subtle problems with mood or mental abilities. In addition 35000 people exhibit some symptoms and 75000 people carry the abnormal gene that will cause them to develop the disease.

Huntingtons disease is a progressive brain disorder caused by a single defective gene on chromosome 4 one of the 23 human chromosomes that carry a persons entire genetic code. Huntingtons disease is a rare inherited disease that causes the progressive breakdown degeneration of nerve cells in the brain. A number of strategies may help people with huntingtons disease and their families cope with the challenges of the disease.

It deteriorates a persons physical and mental abilities usually during their prime working years and has no cure. Support services nonprofit agencies such as the huntingtons disease society of america provide caregiver education referrals to outside services and support groups for people with the disease and caregivers. It gets gradually worse over time and is usually fatal after a period of up to 20 years.

In the united states alone about 30000 people have hd. Huntingtons disease has a broad impact on a persons functional abilities and usually results in movement thinking cognitive and psychiatric disorders. A general lack of coordination and an unsteady gait often follow.

It is a rare genetic disease that impairs physical cognitive and psychological functioning. In japan a much lower prevalence of about one tenth of prevalence of the caucasion population is described recently several phenocopies have been described all of which have an even lower prevalence see paragraph on differential diagnosis. Huntingtons disease hd is a fatal genetic disorder that causes the progressive breakdown of nerve cells in the brain.

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