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Huntington’s disease

    What causes Huntington’s disease?

    Huntington’s disease is a genetic disorder caused by a faulty gene on chromosome 4. A protein called Huntingtin usually helps nerve cells develop but when faulty it can damage them instead and this mainly occurs in the areas of the brain responsible for movement, learning, cognition and emotions (basal ganglia and cerebral cortex). Huntington’s disease is primarily thought of as a condition of motor function – that is, it affects the person’s movement. But there can be damage to the brain which can develop into dementia.

    The first signs of Huntington’s disease are more commonly seen in the 30-50 year age group but current research indicates that about 10% of cases can appear after the age of 60 years and 5-10% of cases under the age of 18 years (known as juvenile Huntington’s disease).

    How does Huntington’s disease develop?

    As the disease progresses people who have Huntington’s are increasingly likely to have involuntary movements causing the characteristic signs (chorea) of Huntington’s disease. This can cause embarrassment, distress, discomfort and social isolation. As the disease progresses it can also cause problems with swallowing, speech, balance and increase the risk of falls.

    Research has indicated that in Huntington’s disease the person’s cognitive processes are also affected and get progressively worse over the years with some people going onto develop dementia in the later stages of Huntington’s. The cognitive changes could include:

    • a reduction in reasoning, judgement, planning and decision-making abilities
    • a change in emotional engagement
    • poor impulse control
    • attention problems
    • difficulty learning new things
    • slowed thinking
    • reduced motivation
    • reduced temper control
    • reduced insight

    The person may also show signs of depression or anxiety.

    Managing the effects of Huntington’s disease

    There is no cure or specific treatment for Huntington’s disease as yet but UK and international research is ongoing. If a family knows they are at increased risk of having the faulty gene they could be offered a DNA test. Only Regional Genetics Clinics offer the testing and access to this is via your GP.

    With Huntington’s disease the interventions are focused on support and management of the changes; working with the person and their family to ensure they can live as well as possible with the condition. The physical effects of Huntington’s disease can be managed by:

    • adapting the home environment so any trip hazards are removed and risks minimised
    • a referral to speech and language therapy if there are speech or swallowing problems
    • a referral to a physiotherapist if there are movement issues
    • a referral to an occupational therapist for aids and devices that may help around the house

    If the person with Huntington’s has significant communication or cognitive issues they can be reduced by:

    • speaking slowly and clearly
    • reducing distractions
    • giving time for communication – it may take longer to respond
    • asking questions to narrow down the answer, give choices or use yes/no cards or picture cards – the person may have word finding difficulties as well as needing longer to respond
    • using a mobile phone, tablet or electronic communication aid
    • providing a routine and activities that the person enjoys and feels comfortable with

    Remember that comprehension can often be well preserved even if the person cannot speak.

    The person with Huntington’s and their family may well have experienced the disease in other family members and have fears about how this will progress and what help and support they may be able to receive. There may also be worries about any children within the family and whether or not they may eventually have Huntington’s too.

    For more information, visit the Huntington’s Disease Association website.

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