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Irritability and depression are common early signs of HD. People may initially be incorrectly diagnosed with psychiatric diseases like schizophrenia and delusional disorder, particularly if they have no other symptoms of HD.

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13y ago
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11y ago

Chorea is a rather archaic term- it is properly called Huntington's Disease. The website for HDSA will provide more info. The external symptoms, which generally do not become apparent until later in life, include problems with voluntary and involuntary movement, including swallowing, changes in personality, problems with memory and reasoning, unsteady walk, slurred speech, etc. The diagnosis of HD is based on a family history of HD, and a genetic screen for the gene that causes it.

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13y ago

Other neurological signs include various abnormal movements, changes in eye movements, difficulty speaking, difficulty swallowing, and increased reflexes.

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13y ago

itchiness, dry eyes. & scaley skin.

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Q: What are the symptoms of Huntington disorder?
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Related questions

What are symptoms of huntington's disease?

Symptoms of Huntington's disease which is a trinucleotide repeat disorder include movement symptoms. These can be seen through clumsiness, clenching of the jaw, loss of coordination, slurred speech and uncontrolled muscle contractions. Then, there are also mental symptoms such as deterioration of judgment and memory which can lead to dementia. Lastly symptoms can include irritability, behavioral changes, and depression.


What age do you get huntington?

Huntington's chorea is a genetic disorder that an affected person is born with. Symptoms usually start when a person is in their 30s or 40s, but sometimes (rarely) it can start when a person is in their 20s. Genetic testing can be done at any age.


Where is Huntington disease found in the body?

Huntington's disease is a genetic disorder. In other words, it runs in the family. It is not contagious. You are born with it and the symptoms show up as you age.


Is huntington disease contagious?

Huntington's disease is not contagious as it is a genetic disorder. It is passed down from parents.


Is huntington's disorder a mutation?

Huntington's disease is a disorder passed down through families in which nerve cells in the brain waste away, or degenerate. Not a mutation. Amber


Is huntington disease a autosomal dominant disorder?

Yes


How does huntington's disease affect the nervous system?

Yes, Huntington's disease is a central nervous system disorder.


Is Hunter Syndrome and Huntington's Chorea the same?

No, Hunter Syndrome (also known as Mucopolysaccharidosis type II) is a rare genetic disorder that affects metabolism. It is caused by the lack of an enzyme in the body. On the other hand, Huntington's chorea (also known as Huntington's disease) is a different genetic disorder that affects the brain, leading to movement, cognitive, and psychiatric symptoms. While both are genetic disorders, they affect different systems in the body.


What is a Co-dominant alleles disorder?

One example is Huntington's Disease. With a recessive genetic disorder, to develop the disorder, you must inherit the gene from BOTH parents (odds, 1 in 4). With a dominant gene disorder, if you inherit the gene from ONE parent, you will develop that disorder (odds- 1 in 2).


What is the nature of bipolar disorder schizophrenia and multiple personalities?

bipolar disorder, mood disorder, symptoms are extremecycles of high and low moodschizophrenia, thought disorder, symptoms are hallucinations and delusionsmultiple personality disorder or dissociative identity disorder, dissociation disorder, symptoms are changes in identity and personality


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 is a hereditary disorder caused by degenerative changes in the cerebrum?

Huntington disease