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多系统萎缩(MSA)症又称进行性系统变性,它主要累及橄榄核、桥脑、小脑、纹状体和黑质,个别病例可累及脊髓侧柱,该病病因不明。为探讨该病是否与氧化反应异常和微量元素有关,现总结如下。 临床资料 本组MSA9例(男6例,女3例),其中2例原发性直立性低血压,4例橄榄桥小脑萎缩,1例纹状体黑质变性,2例多系统变性。年龄40～53岁,平均48.2±4.5岁。 9例病人最早首发症状是时常头晕者2例,无任何诱因晕厥1例,行走不稳或持物
Multi-system atrophy (MSA) also known as progressive systemic degeneration, which mainly affects the olive, pons, cerebellum, striatum and substantia nigra, individual cases may involve the spinal column, the etiology of the disease is unknown. To investigate whether the disease is associated with abnormal oxidation and trace elements, are summarized as follows. Clinical data The group of MSA 9 cases (6 males and 3 females), including 2 cases of primary orthostatic hypotension, 4 cases of Olive Bridge cerebellar atrophy, 1 case of striatonigral degeneration, 2 cases of multiple system degeneration. Aged 40 to 53 years old, with an average of 48.2 ± 4.5 years. The earliest initial symptoms of 9 patients were 2 patients with frequent dizziness, 1 case of syncope without any cause, unstable walking or holding