僵人綜合征什么原因?qū)е拢?/title> <meta name="keywords" content="僵人綜合征什么原因?qū)е? /> <meta name="description" content="僵人綜合征是指一種以軀軸和下肢肌肉過度收縮，伴肌痛性肌肉痙攣為特征的罕見的、嚴重的中樞神經(jīng)系統(tǒng)疾病。那么今天小編在這里給大家整理一下僵人綜合征什么原因?qū)е拢覀円黄鹂纯窗?僵人綜合征病因本病病因可能與"/> <link rel="canonical" href="http://www.yishupeixun.net/"/> <meta http-equiv="Cache-Control" content="no-transform" /> <meta http-equiv="Cache-Control" content="no-siteapp" /> <script src="http://www.yishupeixun.net/public/js/head.js"></script> <link href="/public/css/article.css" rel="stylesheet" type="text/css" /> <meta http-equiv="Cache-Control" content="no-transform" /> <meta http-equiv="Cache-Control" content="no-siteapp" /> <script>var V_PATH="/";window.onerror=function(){ return true; };</script> </head> <body> <h1><a href="http://www.yishupeixun.net/">六月丁香五月婷婷,丁香五月婷婷网,欧美激情网站,日本护士xxxx,禁止18岁天天操夜夜操,18岁禁止1000免费,国产福利无码一区色费</a></h1><div id="rf1n4" class="pl_css_ganrao" style="display: none;"><rp id="rf1n4"></rp><big id="rf1n4"><abbr id="rf1n4"></abbr></big><li 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<div id="e286xo47mbob" class="ar_con_nr"> <div id="e286xo47mbob" class="con_l fl"> <article class="ar_con bg louti"> <div id="e286xo47mbob" class="ar_title"> <h1>僵人綜合征什么原因?qū)е?/h1> <div id="e286xo47mbob" class="ar_title_b"> <div id="e286xo47mbob" class="sub_title clear"> <span id="e286xo47mbob" class="sp2 c6 fl">時間：<time class="fxtime">2024-01-26 12:54:34</time></span> <span id="e286xo47mbob" class="sp1 c6 fl"><em id="zuozhe" class="noshow">自迅</em><em class="user_id noshow">0</em>由 <em class="nickname"></em> 分享</span> <span id="e286xo47mbob" class="fl arc_btn"></span> </div> </div> </div> <div id="e286xo47mbob" class="y_ju"><script type="text/javascript">a("title");</script></div> <div id="e286xo47mbob" class="con_article con_main" id="contentText"> <p>僵人綜合征是指一種以軀軸和下肢肌肉過度收縮，伴肌痛性肌肉痙攣為特征的罕見的、嚴重的中樞神經(jīng)系統(tǒng)疾病。那么今天小編在這里給大家整理一下僵人綜合征什么原因?qū)е?，我們一起看看?</p><p><img alt="僵人綜合征什么原因?qū)е? src="http://uploads2.xuexila.com/yc/20211220/0b19ebde8bd268418a6abd806311ce3e.jpg" width="484" height="300"/></p><h2>僵人綜合征病因</h2><p>本病病因可能與遺傳、神經(jīng)生理、免疫反應等有關。</p><p>1.本病原因雖然不清，但脊髓運動神經(jīng)元持續(xù)興奮，病人尿中去甲腎上腺素代謝產(chǎn)物水平升高，提示中樞神經(jīng)的GABA抑制系統(tǒng)與去甲腎上腺素系統(tǒng)的興奮抑制失平衡可能是本病產(chǎn)生癥狀的原因。</p><p>2.近年來，不少研究提示本病者腦脊髓中募克隆區(qū)帶陽性，lgG合成增加。可能與免疫異常有關，但仍待證實。</p><h2>僵人綜合征臨床表現(xiàn)</h2><p>僵人綜合征起病隱襲，常為慢性波動性，病前常有感染史，病程為5日到4月不等。初期腹部、軀干、肌肉陣發(fā)性酸痛，有緊束感，呈非特異性和一過性，繼而累及四肢。隨著病情進展，常見軀干、四肢及頸部肌肉持續(xù)性或波動性僵硬，腹肌呈板樣或石頭樣堅實，主動肌和對抗肌同時受累。關節(jié)固定，隨意活動受限，嚴重時關節(jié)固定為僵人樣姿勢，國內(nèi)以咀嚼肌多見，其次頸肌首發(fā)。除肌肉僵硬及運動障礙外，少數(shù)可伴錐體束征。癥狀進展，繼之出現(xiàn)腰肌、頸肌、軀干肌及四肢近端肌肉發(fā)緊、僵硬、自主活動限制、行走時挺直不能彎腰等，但是睡眠后僵硬消失。</p><p>陣發(fā)性痛產(chǎn)生痙攣及促發(fā)因素，稍加刺激則可誘發(fā)痛性肢體及腰肌痛性痙攣，被動運動或突然的情感刺激均可誘發(fā)。發(fā)作時病人劇烈疼痛、哭喊、驚恐、大聲嚎叫、出汗、心律不齊等，嚴重者可致骨折或肌肉撕裂。極少累及面部表情肌和咽喉肌。神經(jīng)系統(tǒng)檢查，除肌強直外無異常發(fā)現(xiàn)，智能正常。少數(shù)病人有吞咽困難，呼吸肌受累、胸鎖乳突肌緊張，有的還存情感障礙如抑郁、失眠、幻覺、妄想等。</p><h2>僵人綜合征診斷</h2><p>根據(jù)本病臨床特征，其診斷標準如下：</p><p>1.體軸肌(含面肌、咀嚼肌)持續(xù)僵硬并強直，呈“板樣”(肢體近端肌可受累);</p><p>2.異常的體軸姿勢(常為過度的腰脊柱前凹);</p><p>3.突發(fā)痛性痙攣，由隨意運動、情緒煩亂或未意料的聽覺及體感刺激引起，睡后減輕或消失;</p><p>4.至少在一條體軸機出現(xiàn)持續(xù)的運動單位活動(CMUA);</p><p>5.肌電圖靜息電位可有正常動作電位發(fā)放，發(fā)作時肌電發(fā)放增強，注射安定后電位發(fā)放減弱或消失;</p><p>6.用安定類藥物治療有特效;</p><p>7.應排除腫瘤所致的轉(zhuǎn)移灶。</p><h2>僵人綜合征預防</h2><p>防治呼吸道、泌尿道感染，注意避免聲光刺激，保持情緒穩(wěn)定，預防各種誘發(fā)因素。</p> 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