Huntington's disease

by Dr George El-Nimr and Dr Darren Carr

 

Last reviewed: August 2018

 

Huntington's disease (HD) is a rare genetic disorder affecting the central nervous system. It was described by Dr George Huntington in a paper submitted to the Medical and Surgical Reporter in 1872:

 

'the hereditary chorea, as I shall call it, is confined to certain and fortunately few families, and has been transmitted to them, an heirloom from generation away back in the dim past. It is spoken of by those in whose veins the seed of the disease are known to exist, with a kind of horror, and not at all alluded to except through dire necessity, when it is mentioned as "that disorder". It is attended generally by all the symptoms of common chorea, only in an aggravated degree hardly ever manifesting itself until adult or middle life, and then coming on gradually but surely, by increasing degrees, and often occupying years in its development, until the hapless sufferer is but a quivering wreck of his former self'.

 

While this disease is named after Dr George Huntington, it is important to remember that it was actually described by previous authors; though not as concisely or eloquently!

 

This module will cover the basic neuroscience in relation to this disorder together with the main clinical aspects. Different management strategies and input from different disciplines will also be discussed.

 

Start the module

 

 

If you like this module, you may also be interested in:

 

Young onset dementias by Dr Aijaz Ahmed, Dr Michael Jubb, Dr Rumana Chowdhury and Dr Ben Alderson

 

Alcohol-related brain damage by Professor Kenneth Wilson, Dr Joy Bell and Dr Vanessa Craig

 

An unusual case presentation by Dr Andrew MaCaulay

 

 

 

 

BJPsych Advances: related articles for CPD Online

 

 

Related Advances articles

 

Download take-home notes to print and annotateDownload take-home notes to print and annotate

© 2018 Royal College of Psychiatrists