Huntington's chorea
If youve testing negative. If youre a carer.
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If you have Juvenile Huntingtons.
. Branches and support groups. J Neuropsychiatry Clin Neurosci. If youre at risk.
COVID-19 information and advice hub. HD is typically diagnosed based on clinical findings in the setting of a family history and may be confirmed with genetic testing. Paulsen JS Nehl C Hoth KF Kanz JE Benjamin M Conybeare R McDowell B Turner B.
Living with Huntingtons disease. Huntingtons Disease Society of America 2011. Abnormality of eye movement Abnormality of the cerebral white matter Abnormality of the sense of smell Aggressive behavior Agitation Alcoholism Anxiety Apathy Babinski sign Bradykinesia Caudate atrophy Cerebral atrophy Choking episodes Chorea Clonus Clumsiness Decreased body mass index Degeneration of the striatum Delusions Depressivity.
For children and young people. Depression and stages of Huntingtons disease. If youre an older carer.
Huntingtons disease HD is a dominantly inherited progressive neurological disease characterized by chorea an involuntary brief movement that tends to flow between body regions. If youre showing symptoms. This is an easy-to-read manual on the science and management of Huntingtons disease.
Appropriately chorea is derived from the Greek word khoros meaning dance The extent of the hyperkinesia exhibited in the disease can vary from solely the little finger to the entire body resembling. Hyperkinesia more specifically chorea is the hallmark symptom of Huntingtons disease formerly referred to as Huntingtons chorea.
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