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Huntington's disease

[ huhn-ting-tuhnz di-zeez ]

noun

Pathology.
  1. a hereditary disease of the central nervous system characterized by brain deterioration resulting in involuntary movement and unsteady gait, cognitive impairment and memory decline, and depression or other alterations in mood, with symptoms usually appearing in the fourth decade of life. : HD


Huntington's disease

/ ˈʌԳɪŋə /

noun

  1. a rare hereditary type of chorea, marked by involuntary jerky movements, impaired speech, and increasing dementia Former nameHuntington's chorea
“Collins English Dictionary — Complete & Unabridged” 2012 Digital Edition © William Collins Sons & Co. Ltd. 1979, 1986 © HarperCollins Publishers 1998, 2000, 2003, 2005, 2006, 2007, 2009, 2012
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Word History and Origins

Origin of Huntington's disease1

Named after George S. Huntington (1850–1916), U.S. physician, who described it in 1872
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Word History and Origins

Origin of Huntington's disease1

C19: named after George Huntington (1850–1916), US neurologist
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Example Sentences

Examples have not been reviewed.

Northern Scotland has one of the highest rates of Huntington's disease in the world, according to a new study.

From

The study confirmed the rate of Huntington's disease in northern Scotland is 14.5 per 100,000 people - more than five times the estimated worldwide rate of 2.71.

From

On average, every person who has been diagnosed with Huntington's disease will have at least another 2.2 relatives who have the gene, meaning there are hundreds of people in northern Scotland who could be considered for effective treatments in the future, researchers said.

From

The research was led by Prof Zosia Miedzybrodzka of the University of Aberdeen and clinical lead for Huntington's disease at NHS Grampian, alongside Heather Cruickshank, genetic counsellor at NHS Grampian.

From

"Previous work looked at how many people in the area have been tested for Huntington's disease, that is people diagnosed with Huntington's disease signs and those with a gene alteration that will develop the condition in later life," Prof Miedzybrodzka explained.

From

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