...
首页> 外文期刊>Journal of neurology >Multiple motor system dysfunction associated with a heterozygous ceruloplasmin gene mutation.
【24h】

Multiple motor system dysfunction associated with a heterozygous ceruloplasmin gene mutation.

机译:多运动系统功能障碍与杂合的铜蓝蛋白基因突变有关。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Sirs: Aceruloplasminemia is a rare early-onset autosomal recessive disorder characterized by homozygous or compound heterozygous ceruloplasmin gene mutations, very low to undetectable ceruloplasmin serum levels, anemia, diabetes mellitus, retinal degeneration, cerebellar ataxia, dystonia and dementia . The heterozygous condition, familial hypoceruloplasmin-emia, has been largely considered an incidental finding. We describe a patient with hypoceruloplasmin-emia and a novel heterozygous ceruloplasmin gene mutation with the aim to better define the clinical spectrum of this entity.The patient is a 33-year-old woman with an unremarkable medical history. Her parents are healthy and non-consanguineous. She has two healthy brothers. She presented at the age of 26 years with dysarthria, followed by slowly progressive gait ataxia, and mandibular and cervical dystonia. Current examination showed scanning speech, left lat-erocollis, mild paraparesis and leg incoordination, diffuse hyperre-flexia, bilateral extensor plantar responses, and an ataxic and spastic gait.
机译:主席先生:血浆铜蓝蛋白血症是一种罕见的早发型常染色体隐性遗传病,其特征是纯铜或复合杂合铜蓝蛋白基因突变,血清铜蓝蛋白水平极低至无法检测,贫血,糖尿病,视网膜变性,小脑性共济失调,肌张力障碍和痴呆。杂合子病,家族性次要铜血纤维蛋白溶酶血症,在很大程度上被认为是偶然发现。我们描述了一名患有低铜蓝蛋白血症和新的杂合铜蓝蛋白基因突变的患者,旨在更好地定义该实体的临床范围。该患者是一名33岁的女性,病史不明显。她的父母很健康,没有血缘关系。她有两个健康的兄弟。她现年26岁,患有构音障碍,随后出现缓慢进行性步态共济失调,下颌和颈肌张力障碍。当前检查显示语音扫描,左横结肠,轻度轻瘫和小腿不协调,弥漫性反射亢进,双侧伸肌足底反应以及共济和痉挛性步态。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号