huntington’s disease an overview
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Huntington’s Disease An Overview. Huntington’s Disease Association Dee Boyd – Regional Care Advisor. Contents. What is HD? Statistics Genetics Symptoms. What is Huntington’s disease?. A hereditary degenerative neuro-psychiatric disorder - PowerPoint PPT PresentationTRANSCRIPT
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Huntington’sHuntington’s Disease Disease An OverviewAn Overview
Huntington’s Disease AssociationDee Boyd – Regional Care Advisor
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Contents
• What is HD?• Statistics• Genetics• Symptoms
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What is Huntington’s disease?
• A hereditary degenerative neuro-psychiatric disorder
• Symptoms of HD usually start between the ages of 30-50 years, although late onset and juvenile manifestation does occur
• The prognosis is usually between 15-20 years from onset of symptoms
• Currently no cure
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Statistics
• 6,000 -10,000 – in the population of the UK• 1in 10,000
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Genetics
• An inherited dominant genetic condition caused by a mutation on chromosome 4
• Each child of an affected parent has a 50:50 chance of inheriting the gene and therefore developing the disease at some stage
• Identified the gene in 1989 and a predictive test has been available from 1993
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• Huntington’s disease affects the whole family• It can have an effect on generations• Sometimes a person who has the HD gene dies
before any symptoms appear. The gene may have been passed on without anyone realising it is in the family
• Anyone who inherits the gene will develop the disease unless they die before this happens
Implications
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Physical problems
Cognitiveproblems
Emotional problems
These problems interact with each other
A Triad of problems with Huntington’s disease
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Healthy vs. HD Brain
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Typical Physical Changes
• Chorea - Often starts with fidgety movements • Might seem clumsy or stumble more than
usual • Over time movements tend to become more
noticeable• Voluntary movements also affected• Rigidity
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Typical Physical Changes
• Speech might sound a bit slurred• Lack of control of volume • As the disease progresses, swallowing
problems are common• Weight Loss• Incontinence
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Typical Cognitive Changes• Harder to plan and think ahead• Harder to switch from one task to another• Prefer a set routine, and want things done in a
certain way and immediately. Change to routine can cause anxiety or frustration
• Changes in behaviour may be due to medication, pain, temperature, visitors, staff, fatigue, processing skills, frustration and overload
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Typical Cognitive Changes
• Lack of motivation – appear lazy• Memory and concentration problems• Inability to recognise they have a problem• Denial – or is it?• Reduced ability to read facial expression• Inability to adapt behaviour• Extra processing time is required. Longer to
receive an answer
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Typical Emotional Changes
• Cognitive changes lead to frustration which in turn lead to temper outbursts
• Emotional changes often start with subtle changes to mood / behaviour
• Some people become aggressive, demanding, stubborn and self-centred.
• Depression is common, but very treatable
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Typical Emotional Changes
• Again because of cognitive changes people can be impulsive or irrational, behaving in a disinhibited way or obsessive with things
• These may lead to social isolation
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Points to remember
• Some people with Huntington’s disease can experience mental health issues
• People with HD are individuals and will differ in the extent and sequence with which they experience symptoms
• However, although people may move in and out of the stages, there are broad developments during the progress of the disease
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Other considerations
• HD can make a person more difficult to live with
• Relationship changes• Not the person I married• Loss and bereavement
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Salient Points
• Huntington’s Disease can be considered as a veil. Sometimes you can see through the veil
• The movement disorder is the most apparent• The mental health/behavioural aspects are
the most worrisome• The cognitive impairment is the most disabling• Huntington’s Disease affects every individual
in a unique way
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Further Reading
• Huntington’s Disease Association Fact Sheets• A range of other books, leaflets and resources
available via the HDA Website and Head Office
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Huntington’s Disease Association
• For more information contact Head Office
Suite 24Liverpool Science CentreI31 Mount PleasantLiverpool L3 5TF
Tel: 0151 331 5444
E mail: [email protected]
Web: www.hda.org.uk