Treatable inherited rare movement disorders

• Published in: Movement disorders Vol. 33; no. 1; pp. 21 - 35
• Main 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.
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.01.2018
• Subjects: Clinical trials; Clinical Trials as Topic - methods; Dihydroxyphenylalanine; Dystonia; experimental therapeutics; Humans; inherited disease; Movement disorders; Movement Disorders - genetics; Movement Disorders - therapy; orphan disease; Parkinson's disease; Rare disease; Rare Diseases - genetics; Rare Diseases - therapy; treatment; Treatment Outcome; Wilson's disease; inherited disease; orphan disease; treatment; experimental therapeutics; Rare disease

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 mechani...