...
首页> 外文期刊>International Neuropsychiatric Disease Journal >Familial Idiopathic Basal Ganglia Calcification (Fahr's syndrome): Initial Clinical Neuropsychiatric Presentation without Corresponding Neurological Deficit
【24h】

Familial Idiopathic Basal Ganglia Calcification (Fahr's syndrome): Initial Clinical Neuropsychiatric Presentation without Corresponding Neurological Deficit

机译:家族性特发性基底神经节钙化(Fahr综合征):最初的临床神经精神病学表现,而没有相应的神经功能缺损

获取原文

摘要

Familial idiopathic basal ganglia calcification (FIBGC) or Fahr's syndrome is a rare disorder with various clinical presentations which can mimic - in particular - psychiatric illness. The following case is characterized by the typical basal ganglia calcifications and presentation of neuropsychiatric symptoms indicating the first clinical presentation in the absence of a neurological deficit. As previously reported, the extent of calcification did not predict neurological impairment, however, predicted severe psychosis.
机译:家族性特发性基底神经节钙化(FIBGC)或Fahr综合征是一种罕见的疾病,具有多种临床表现,可以模仿特别是精神病。以下病例的特征是典型的基底神经节钙化和神经精神症状的表现,表明在没有神经功能缺损的情况下首次临床表现。如先前报道,钙化程度不能预示神经功能障碍,但是预示严重精神病。

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