Huntington's disease is a genetically inherited condition which results
in severe nerve-cell damage in the brain. The hereditary and
debilitative nature of the disease means that many people are involved
either directly or indirectly by this condition.
This book has been written for patients and the families and carers of
people with Huntington's disease (HD). It provides an accessible
introduction to the condition that explains the physical, behavioural,
and emotional features of the disease, the important role of genetics
and options for those
at risk of developing the condition, plus advice on managing and
treating symptoms. Patient perspectives are included throughout,
offering real-life accounts from people who have or know someone with
the condition.
This new edition has been fully updated to include all the latest
research in HD. It gives more detail on the standard treatments, as well
as explaining new trials aimed at reducing the level of the abnormal
protein (huntingtin) in the brains of patients.