進行性核上麻痹患者的頭部MRI表現(xiàn)
發(fā)布時間：2019-02-13 10:22
【摘要】：正進行性核上麻痹(progressive supranuelear palsy,PSP)是一種少見的神經(jīng)系統(tǒng)變性疾病,主要臨床表現(xiàn)有垂直性凝視麻痹、軸性肌張力障礙、跌倒、球麻痹、癡呆等;病理表現(xiàn)為累及皮質(zhì)、中腦、腦干、基底核和小腦的一種微管相關(guān)蛋白(tau)蛋白病~([1])。PSP起病隱匿,早
[Abstract]:Progressive supranuclear paralysis (progressive supranuelear palsy,PSP) is a rare neurodegenerative disease with the main clinical manifestations of vertical staring paralysis, axial dystonia, falls, bulbar paralysis, dementia and so on. A microtubule-associated protein (tau) protein involved in the cortex, midbrain, brainstem, basal nucleus and cerebellum is characterized by occult and early onset of ~ (1). PSP.
【作者單位】： 寧波市醫(yī)療中心李惠利東部醫(yī)院神經(jīng)內(nèi)科;
【分類號】：R742
[Abstract]:Progressive supranuclear paralysis (progressive supranuelear palsy,PSP) is a rare neurodegenerative disease with the main clinical manifestations of vertical staring paralysis, axial dystonia, falls, bulbar paralysis, dementia and so on. A microtubule-associated protein (tau) protein involved in the cortex, midbrain, brainstem, basal nucleus and cerebellum is characterized by occult and early onset of ~ (1). PSP.
【作者單位】： 寧波市醫(yī)療中心李惠利東部醫(yī)院神經(jīng)內(nèi)科;
【分類號】：R742
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1 王雪晴;林子玲;劉漢偉;張雷;周武;韓蓉蓉;;進行性核上性麻痹3例臨床特點[J];中國臨床研究;2010年09期
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