Treatable inherited rare movement disorders

Research output: Contribution to journalReview article

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.

Details

Authors
  • H. A. Jinnah
  • Alberto Albanese
  • 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-Violante
  • Ludger Schöls
  • Maria Stamelou
  • Marina Tijssen
  • Claudia Uribe Roca
  • Andres de la Cerda
  • Emilia M. Gatto
  • for the International Parkinson's Disease Movement Disorders Society Task Force on Rare Movement Disorders
External organisations
  • Emory University
  • Humanitas Research Hospital
  • Catholic University of the Sacred Heart, Milan
  • University College London
  • Federal University of Minas Gerais
  • University of Buenos Aires
  • University del Salvadore
  • University Medical Center Groningen
  • University of Cincinnati
  • University of Sydney
  • Hospital Fundación Jiménez Díaz
  • Favaloro Foundation University Hospital
  • Baylor College of Medicine
  • Tokushima University
  • St. Vincent's Health
  • University of Toronto
  • University of Alberta
  • University of Messina
  • British Columbia Children's Hospital
  • National Institute of Mental Health and Neurosciences, Bangalore
  • Hospital Universitario Donostia
  • Basque Center on Cognition, Brain and Language
  • Basque Foundation for Science
  • CIBER Enfermedades Neurodegenerativas (CIBERNED)
  • Instituto Nacional de Neurología y Neurocirugía
  • University of Tübingen
  • German Center for Neurodegenerative Diseases (DZNE), Bonn
  • Philipp University of Marburg
  • Hygeia Hospital
  • British Hospital of Buenos Aires
  • Universidad de los Andes, Chile
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Neurology

Keywords

  • experimental therapeutics, inherited disease, orphan disease, Rare disease, treatment
Original languageEnglish
Pages (from-to)21-35
Number of pages15
JournalMovement Disorders
Volume33
Issue number1
Publication statusPublished - 2018 Jan 1
Publication categoryResearch
Peer-reviewedYes
Externally publishedYes