Huntington's disease


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Hun·ting·ton's disease

 (hŭn′tĭng-tənz)
n.
A rare inherited disease of the central nervous system characterized by progressive dementia, abnormal posture, and involuntary movements. The typical age of onset is between 30 and 50 years. Also called Huntington's chorea.

[After George Huntington (1851?-1916), American physician.]

Huntington's disease

(ˈhʌntɪŋtən)
n
(Pathology) a rare hereditary type of chorea, marked by involuntary jerky movements, impaired speech, and increasing dementia. Former name: Huntington's chorea
[C19: named after George Huntington (1850–1916), US neurologist]
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.Huntington's disease - hereditary disease; develops in adulthood and ends in dementia
monogenic disease, monogenic disorder - an inherited disease controlled by a single pair of genes
chorea - any of several degenerative nervous disorders characterized by spasmodic movements of the body and limbs
autosomal dominant disease, autosomal dominant disorder - a disease caused by a dominant mutant gene on an autosome
References in periodicals archive ?
This is particularly intriguing as this process has not been implicated in Huntington's disease in the past.
Trehalose joins a growing list of potential Huntington's disease fighters (SN: 2/15/03, p.
Tress Padellford, 23, another student in the program, said that in the course of her field work she had to counsel people whose parents developed Huntington's disease.
with a third of its beds reserved for patients with Huntington's disease.
Earlier this year, Gavin Newlands, MP for Paisley and Renfrewshire North, led a debate in parliament on the challenges that people with Huntington's disease and those at risk from it have in accessing insurance.
Patients with Huntington's disease develop a toxic protein called mutant huntingtin which slowly "poisons" specific groups of brain cells, typically over a 15 or 20-year period.
Israeli pharmaceutical firm Teva (TLV: TEVA)'s Austedo has become the first and only Huntington's disease medication that treats both tardive dyskinesia and chorea to be approved in the US, the company said on Wednesday.
Huntington's disease is a fatal genetic disorder that causes the progressive breakdown of nerve cells in the brain.
Huntington's disease is an inherited disease that causes the progressive breakdown (degeneration) of nerve cells in the brain.
Often known as Huntington's chorea because of the movement problems it causes, Huntington's disease is an inherited condition that damages certain nerve cells in the brain and leads to problems with mobility, thinking and perception.
The Institute of Neurology and Genetics said in a statement it supports the international effort to raise awareness of Huntington's disease and is co-operating with Cypriot, European and world associations involved in various public awareness events.
The Huntington's Disease EpiCast Report provides an overview of the risk factors, comorbidities, and global trends for Huntington's disease (HD) in the seven major markets (7MM) (US, France, Germany, Italy, Spain, UK, and Japan).

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