Diagnosis and Treatment of Chorea Syndromes

被引:53
作者
Hermann, Andreas [1 ,2 ]
Walker, Ruth H. [3 ,4 ]
机构
[1] Tech Univ Dresden, Div Neurodegenerat Dis, Dept Neurol, D-01307 Dresden, Germany
[2] German Ctr Neurodegenerat Dis DZNE Dresden, D-01307 Dresden, Germany
[3] James J Peters Vet Affairs Med Ctr, Dept Neurol, 130 W Kingsbridge Rd, Bronx, NY 10468 USA
[4] Mt Sinai Sch Med, Dept Neurol, New York, NY 10029 USA
关键词
Chorea; Huntington's disease; Basal ganglia; Neuroacanthocytosis; Huntington disease-like; BENIGN HEREDITARY CHOREA; DEEP BRAIN-STIMULATION; TERM-FOLLOW-UP; DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY; PAROXYSMAL KINESIGENIC DYSKINESIA; HUNTINGTONS-DISEASE; MOVEMENT-DISORDERS; PHARMACOLOGICAL-TREATMENT; DIFFERENTIAL-DIAGNOSIS; RECEPTOR ENCEPHALITIS;
D O I
10.1007/s11910-014-0514-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chorea is a common movement disorder which can be caused by a large variety of diseases including neurodegenerative diseases, metabolic diseases, and autoimmune diseases, or can be secondary to structural changes. The basal ganglia seem to be mainly involved in the pathophysiology indicating the vulnerability of this region. The diagnosis can be challenging, especially if chorea occurs during the treatment of neuropsychiatric conditions, and in these cases, it is difficult to distinguish between medication side effects (i.e., tardive dyskinesia) and the development of a neurodegenerative disease. Most therapeutic approaches are predominantly symptomatic, with a focus on multidisciplinary care for many patients. Nevertheless, some underlying diseases can be successfully treated and must not be missed. In this review, we summarize recent new developments in the differential diagnosis of chorea syndromes and suggest a pathway for a successful diagnosis of chorea in infancy, childhood, and adulthood for daily practice.
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页数:12
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