舞蹈病-棘状红细胞增多症1例

• 作 者: 谢首佳 胡俊 陈康宁 史树贵
• 机 构: 第三军医大学西南医院神经内科,
• 出 处: 第三军医大学学报
• 发表日期: 2013年19期
• 关键词: 棘状红细胞增多 言语不清 棘红细胞增多 鉴别诊断 舌咬伤 不自主运动 牙齿磨损 临床资料 构音障碍 吞咽困难

舞蹈病-棘状红细胞增多症(chorea-acanthocytosis,ChAc)是一种罕见的常染色体隐性遗传病。常伴有棘红细胞增多,主要临床表现为突发的、不规则的、类似亨廷顿舞蹈病样的不自主运动以及特征性的口面部不自主运动,常导致牙齿磨损、舌咬伤、发出怪声、构音障碍等。本科诊治1例,现报告如下。1临床资料患者,女性,36岁,因“言语不清、行走不稳3年余,加重半年”于2012年10月7日入院。患者于3年前无明显诱因出现

Chorea - Chorea-acanthocytosis (ChAc) is a rare autosomal recessive disease. Often accompanied by increased erythrocytes, the main clinical manifestations of sudden, irregular, similar to Huntington’s disease-like involuntary movement and the characteristic facial movements involuntary movement, often lead to tooth wear, tongue bites, strange sound , Dysarthria and so on. Undergraduate diagnosis and treatment of a case, are as follows. 1 Clinical data Patients, female, 36 years old, due to “illiterate, walking more than 3 years, aggravating six months ” on October 7, 2012 admission. Patients had no obvious incentive 3 years ago