Treatable inherited rare movement disorders. Issue 1 (1st September 2017)
- Record Type:
- Journal Article
- Title:
- Treatable inherited rare movement disorders. Issue 1 (1st September 2017)
- Main Title:
- Treatable inherited rare movement disorders
- Authors:
- Jinnah, H. A.
Albanese, Alberto
Bhatia, Kailash P.
Cardoso, Francisco
Da Prat, Gustavo
de Koning, Tom J.
Espay, Alberto J.
Fung, Victor
Garcia‐Ruiz, Pedro J.
Gershanik, Oscar
Jankovic, Joseph
Kaji, Ryuji
Kotschet, Katya
Marras, Connie
Miyasaki, Janis M.
Morgante, Francesca
Munchau, Alexander
Pal, Pramod Kumar
Rodriguez Oroz, Maria C.
Rodríguez‐Violante, Mayela
Schöls, Ludger
Stamelou, Maria
Tijssen, Marina
Uribe Roca, Claudia
de la Cerda, Andres
Gatto, Emilia M. - Abstract:
- ABSTRACT: There are many rare movement disorders, and new ones are described every year. Because they are not well recognized, they often go undiagnosed for long periods of time. However, early diagnosis is becoming increasingly important. Rapid advances in our understanding of the biological mechanisms responsible for many rare disorders have enabled the development of specific treatments for some of them. Well‐known historical examples include Wilson disease and dopa‐responsive dystonia, for which specific and highly effective treatments have life‐altering effects. In recent years, similarly specific and effective treatments have been developed for more than 30 rare inherited movement disorders. These treatments include specific medications, dietary changes, avoidance or management of certain triggers, enzyme replacement therapy, and others. This list of treatable rare movement disorders is likely to grow during the next few years because a number of additional promising treatments are actively being developed or evaluated in clinical trials. © 2017 International Parkinson and Movement Disorder Society
- Is Part Of:
- Movement disorders. Volume 33:Issue 1(2018)
- Journal:
- Movement disorders
- Issue:
- Volume 33:Issue 1(2018)
- Issue Display:
- Volume 33, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 33
- Issue:
- 1
- Issue Sort Value:
- 2018-0033-0001-0000
- Page Start:
- 21
- Page End:
- 35
- Publication Date:
- 2017-09-01
- Subjects:
- Rare disease -- orphan disease -- inherited disease -- treatment -- experimental therapeutics
Movement disorders -- Periodicals
610 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8257 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mds.27140 ↗
- Languages:
- English
- ISSNs:
- 0885-3185
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5980.317200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 8794.xml