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[特发性血色素沉着症中的锥体外系综合征。实验室化学检查、神经生理学检查及影像学检查(计算机断层扫描、磁共振成像)的意义]

[Extrapyramidal syndrome in idiopathic hemochromatosis. Significance of laboratory chemical, neurophysiologic and imaging procedures (CCT, MRT)].

作者信息

Schröder J, Haan J

机构信息

Neurologische Klinik, Ruhr-Universität am St. Josef-Hospital, Bochum.

出版信息

Nervenarzt. 1987 Sep;58(9):577-8.

PMID:3670519
Abstract

In any patient with unexplained basal ganglia symptoms or dementia, the possibility of idiopathic hemochromatosis (IHC) should be considered. The findings of magnetic resonance tomography, discussed in this case report, lead to the conclusion that IHC is very likely to induce these syndromes. This is of clinical importance as IHC can be successfully treated by phlebotomy.

摘要

对于任何有不明原因的基底节症状或痴呆的患者,都应考虑特发性血色素沉着症(IHC)的可能性。本病例报告中讨论的磁共振断层扫描结果得出结论,IHC很可能诱发这些综合征。这具有临床重要性,因为IHC可通过放血疗法成功治疗。

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Nervenarzt. 1987 Sep;58(9):577-8.
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Quantitative T2* magnetic resonance imaging for evaluation of iron deposition in the brain of β-thalassemia patients.定量 T2* 磁共振成像评估β-地中海贫血患者脑内铁沉积。
Clin Neuroradiol. 2012 Sep;22(3):211-7. doi: 10.1007/s00062-011-0108-z. Epub 2011 Dec 13.
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Movement disorder due to aceruloplasminemia and incorrect diagnosis of hereditary hemochromatosis.由于血浆铜蓝蛋白缺乏症导致的运动障碍以及遗传性血色素沉着症的误诊
J Neurol. 2007 Jan;254(1):113-4. doi: 10.1007/s00415-006-0289-6. Epub 2007 Feb 14.
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Chronic cerebellar ataxia and hereditary hemochromatosis: causal or coincidental association?
慢性小脑性共济失调与遗传性血色素沉着症:因果关联还是偶然关联?
J Neurol. 2007 Sep;254(9):1296-7. doi: 10.1007/s00415-006-0507-2. Epub 2007 Apr 21.
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Hereditary hemochromatosis and movement disorders: the still controversial relationship. Response to Russo et al. in J Neurol (2004) 251:849-852.遗传性血色素沉着症与运动障碍:仍具争议的关系。对鲁索等人发表于《神经病学杂志》(2004年)第251卷第849 - 852页文章的回应
J Neurol. 2006 Feb;253(2):261-2. doi: 10.1007/s00415-005-0954-1. Epub 2005 Aug 17.
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Hereditary haemochromatosis is unlikely to cause movement disorders--a critical review.遗传性血色素沉着症不太可能导致运动障碍——一项批判性综述。
J Neurol. 2004 Jul;251(7):849-52. doi: 10.1007/s00415-004-0445-9.