Palliative care for patients with MND/ALS

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Ressource 1Download: BIB_6D83293F5778.P001.pdf (69.77 [Ko])
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Version: author
Serval ID
serval:BIB_6D83293F5778
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Title
Palliative care for patients with MND/ALS
Journal
European Journal of Palliative Care
Author(s)
Oliver D., Borasio G.D.
ISSN
1352-2779
Publication state
Published
Issued date
2004
Volume
11
Number
5
Pages
185-187
Language
english
Notes
pdf type: clinical management
Abstract
Motor neurone disease (amyotrophic lateral sclerosis) is a relatively rare progressive, degenerative neurological disease with a prevalence of about 7 per 100,000 population. The cause is usually unknown, although in about 5% there is a family history and of these in 20% (that is, 1% of the total MND/ALS population) an abnormal gene can be found - the superoxide dismutase 1 gene on chromosome 21. There is no curative treatment but the glutamate blocker, riluzole, has been shown in trials to reduce the rate of progression and may extend life by a few months. The prognosis is in the order of three to five years.
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24/01/2014 11:16
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20/08/2019 15:27
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