Treatable inherited rare movement disorders

Alberto Albanese, H. A. Jinnah, Kailash P. Bhatia, Francisco Cardoso, Gustavo Da Prat, Tom J. De Koning, Alberto J. Espay, Victor Fung, Pedro J. Garcia-Ruiz, Oscar Gershanik, Joseph Jankovic, Ryuji Kaji, Katya Kotschet, Connie Marras, Janis M. Miyasaki, Francesca Morgante, Alexander Munchau, Pramod Kumar Pal, Maria C. Rodriguez Oroz, Mayela Rodríguez-ViolanteLudger Schöls, Maria Stamelou, Marina Tijssen, Claudia Uribe Roca, Andres De La Cerda, Emilia M. Gatto

Risultato della ricerca: Contributo in rivistaArticolo in rivistapeer review

38 Citazioni (Scopus)

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.
Lingua originaleEnglish
pagine (da-a)21-35
Numero di pagine15
RivistaMovement Disorders
Volume33
DOI
Stato di pubblicazionePubblicato - 2018

Keywords

  • Neurology
  • Neurology (clinical)
  • Rare disease
  • experimental therapeutics
  • inherited disease
  • orphan disease
  • treatment

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