2009British Journal of Healthcare AssistantsRequires access

Huntington's disease part 1: what is it?

Mark Baker, Daniela Blumlein

Open publisher page 5 citations

Abstract

This is the first in a two-part series on Huntington's disease (HD). Part one describes what the neurological disease is and how it affects sufferers. HD is a progressive genetic neurological disease which affects approximately 6.2 in 100000 adults within the UK (Orphanet, 2008). HD is a hereditary disorder of the central nervous system. It used to be known as Huntington's chorea. Huntington's disease usually develops in adulthood and can cause a very wide range of symptoms (Huntingdon's Disease Association, 2008).

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What this paper is about

This is the first in a two-part series on Huntington's disease (HD). Part one describes what the neurological disease is and how it affects sufferers. HD is a progressive genetic neurological disease which affects approximately 6.2 in 100000 adults within the UK (Orphanet, 2008). HD is a hereditary disorder of the central nervous system. It used to be known as Huntington's chorea. Huntington's disease usually develops in adulthood and can cause a very wide range of symptoms (Huntingdon's Disease Association, 2008).

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Available abstract

This is the first in a two-part series on Huntington's disease (HD). Part one describes what the neurological disease is and how it affects sufferers. HD is a progressive genetic neurological disease which affects approximately 6.2 in 100000 adults within the UK (Orphanet, 2008). HD is a hereditary disorder of the central nervous system. It used to be known as Huntington's chorea. Huntington's disease usually develops in adulthood and can cause a very wide range of symptoms (Huntingdon's Disease Association, 2008).

Key concepts: Chorea, Huntington's disease, Disease, Genetic disorder, Medicine, Psychiatry, Psychology, Neuroscience

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