Sobell Department of Motor Neuroscience and Movement Disorders, UCL, Institute of Neurology, Queen Square, London, United Kingdom.
Mov Disord. 2010 Jul 30;25(10):1487-91. doi: 10.1002/mds.23052.
Chorea-acanthocytosis is a rare autosomal recessive neurodegenerative disorder with a complex clinical presentation comprising of a mixed movement disorder (mostly chorea and dystonia), seizures, neuropathy and myopathy, autonomic features as well as dementia and psychiatric features. Because the differential diagnosis is wide, clinical clues and red flags are important. We report here our observation of characteristic neck and trunk flexion and extension spasms in four cases with advanced chorea-acanthocytosis.
舞蹈棘红细胞增多症是一种罕见的常染色体隐性神经退行性疾病,具有复杂的临床表现,包括混合运动障碍(主要是舞蹈症和肌张力障碍)、癫痫、周围神经病和肌病、自主神经特征以及痴呆和精神特征。由于鉴别诊断范围广泛,临床线索和警示征象很重要。我们在此报告了我们观察到的 4 例晚期舞蹈棘红细胞增多症患者的特征性颈部和躯干屈伸痉挛。