Friday, November 24, 2017

Huntington's Disease

Find sites offering information, advice and assistance. Huntington's disease affects muscle coordination and is caused by a faulty gene on chromosome 4. This gene produces a protein called Huntingtin that can lead to damage of the nerve cells in the brain. Children of parent that have Huntington's disease have a 50-50 chance of inheriting the gene. Huntington's disease symptoms are abnormal or disabling body movements called chorea and can result in a severe lack of coordination. Find official and unofficial Huntington's disease facts, symptoms diagnosis, treatment and causes details listed in the sites below and click on the individual titles to visit each website.


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Number of listings: 8
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HD Clinical Research

Highlights current and future clinical research projects into the causes and treatment of Huntington’s disease.

Huntington's Disease and Youth Organisation

Providing a comprehensive broad selection of Huntington's disease information and resources including a discussion forum and numerous links of interest.

Huntington's Disease Association Northern Ireland

Providing advice and support as well as details of ongoing research into Huntington's disease. Includes contacts and donation details.

Huntington's Disease Support Club

An online discussion forum organising scheduled chat three times a week for people suffering from or affected by Huntington's disease.

Medice Plus: Huntington's Disease

Offers an overview of huntington's disease with background details and how to spot early symptoms.

NHS Choices: Huntington's

Official Huntington's disease information from the NHS with details of who is affected, causes and the symptoms. Includes a video clip.

Scottish Huntington's Association

Established and run by families living with Huntington’s disease in Scotland. Offers information and resources with fundraising details and contacts for advice.

The Huntington's Disease Association

Offers support to anybody affected by the disease along with information and advice to professionals that work to support Huntington's disease families.