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This is because about 90% of people with HD have chorea. These movements may be mild at first, but can worsen and become more involuntary with time.

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14y ago

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What is other name for huntingtons disease?

Huntington's Chorea


Is huntingtons chorea the same as huntingtons disease?

Yes. The involuntary movements of Huntington's were thought to resemble a kind of dance (chorea - like choreograph).


What is a similar disease to Huntington's disease?

Huntington's Chorea


Is Parkinsons chorea related to Huntingtons disease in men?

No.


In Huntington's Disease or Huntington's Chorea what is the microbe called?

There IS no microbe. HD is a genetically transmitted disease- you can't catch it.


This famous folk singer died of a disease called huntington's chorea or huntington's disease?

AnswerHuntington's Disease and Huntington's Chorea are essentially one and the same. Chorea is a greek term used to define the uncontrollable movements a person might have with any number of neurological diseases. Huntington's Disease is what took his life.


Is Huntington's disease curable?

No but it is a very slow and unpainful processno sadly huntingtons disease(also known as huntingtons chorea) has no known cure.


What is the hereditary disorder that causes the irreversible and progressive loss of muscle control and mental ability?

Huntington's Disease or Huntington's Chorea


How can you get Huntington's Chorea?

Chorea is an old name for Huntington's Disease. It is genetically transmitted from parent to child. The only way to get HD is to inherit the gene that causes it from one of your parents that also had HD.


What is the history behind the name Huntington WV?

huntington's Disease was first recognised as an inherited disorder in 1872 when a 22-year-old American doctor, George Huntington, wrote a paper called On Chorea. His paper was later published in the Medical and Surgical Reporter of Philadelphia and the disorder he described became known as Huntington's Chorea.


What are the main features of huntingtons chorea?

Huntington's chorea, also known as Huntington's disease, is characterized by progressive motor dysfunction, including involuntary jerking or writhing movements (chorea), as well as cognitive decline and psychiatric symptoms. Patients often experience behavioral changes, mood swings, and difficulties with coordination and balance. The disease typically manifests in mid-adulthood and is caused by a genetic mutation in the HTT gene, leading to neurodegeneration, particularly in the basal ganglia. As the disease progresses, individuals may face significant challenges in daily functioning and require increasing levels of care.


Why do they call it Huntington's Chorea?

Huntington disease is also called Huntington chorea, from the Greek word for "dance," referring to the involuntary movements that develop as the disease progresses. It is occasionally referred to as "Woody Guthrie disease" for the American folk singer who died from it. Huntington disease (HD) causes progressive loss of cells in areas of the brain responsible for some aspects of movement control and mental abilities. A person with HD gradually develops abnormal movements and changes in cognition (thinking), behavior and personality.