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去铁胺在无铜蓝蛋白血症治疗中的应用。

Use of desferrioxamine in the treatment of aceruloplasminemia.

作者信息

Miyajima H, Takahashi Y, Kamata T, Shimizu H, Sakai N, Gitlin J D

机构信息

First Department of Medicine, Hamamatsu University School of Medicine, Japan.

出版信息

Ann Neurol. 1997 Mar;41(3):404-7. doi: 10.1002/ana.410410318.

Abstract

Aceruloplasminemia is a newly recognized autosomal recessive disorder of iron metabolism resulting in neurodegeneration of the retina and basal ganglia. We report here on the treatment of a patient who developed progressive extrapyramidal symptoms that included blepharospasm, grimacing, and rigidity associated with increased iron deposition in the brain and visceral organs. Treatment for 10 months with the iron chelator desferrioxamine decreased brain iron stores, prevented progression of the neurological symptoms, and reduced plasma lipid peroxidation. These data suggest that early treatment with this chelator may be useful in such patients to diminish central nervous system iron accumulation and to prevent or ameliorate neurological symptoms associated with neurodegeneration.

摘要

无铜蓝蛋白血症是一种新发现的常染色体隐性铁代谢紊乱疾病,可导致视网膜和基底神经节神经变性。我们在此报告一位患者的治疗情况,该患者出现了进行性锥体外系症状,包括眼睑痉挛、鬼脸样动作和强直,同时伴有大脑和内脏器官铁沉积增加。使用铁螯合剂去铁胺治疗10个月后,脑铁储备减少,神经症状进展得到预防,血浆脂质过氧化水平降低。这些数据表明,对这类患者早期使用这种螯合剂可能有助于减少中枢神经系统铁蓄积,并预防或改善与神经变性相关的神经症状。

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