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Oromandibular Dystonia in Wilson's Disease.威尔逊病中的口下颌肌张力障碍
Mov Disord Clin Pract. 2015 May 9;2(3):253-259. doi: 10.1002/mdc3.12171. eCollection 2015 Sep.
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A Study on Apoptosis and Anti-apoptotic Status in Wilson Disease.肝豆状核变性的细胞凋亡与抗凋亡状态研究
Mol Neurobiol. 2016 Dec;53(10):6659-6667. doi: 10.1007/s12035-015-9570-y. Epub 2015 Dec 8.
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A study of MRI changes in Wilson disease and its correlation with clinical features and outcome.肝豆状核变性的MRI变化及其与临床特征和预后的相关性研究
Clin Neurol Neurosurg. 2015 Nov;138:31-6. doi: 10.1016/j.clineuro.2015.07.013. Epub 2015 Jul 21.
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Role of Oxidative Stress in the Worsening of Neurologic Wilson Disease Following Chelating Therapy.氧化应激在螯合治疗后神经型威尔逊病病情恶化中的作用。
Neuromolecular Med. 2015 Dec;17(4):364-72. doi: 10.1007/s12017-015-8364-8. Epub 2015 Jul 30.
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Utility of the Midbrain Tegmentum Diameter in the Differential Diagnosis of Progressive Supranuclear Palsy from Idiopathic Parkinson's Disease.中脑被盖直径在进行性核上性麻痹与特发性帕金森病鉴别诊断中的应用
J Clin Neurol. 2015 Jul;11(3):268-74. doi: 10.3988/jcn.2015.11.3.268.
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A study of oxidative stress, cytokines and glutamate in Wilson disease and their asymptomatic siblings.一项关于威尔逊病及其无症状同胞的氧化应激、细胞因子和谷氨酸的研究。
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Samuel Alexander Kinnier Wilson. Wilson's disease, Queen Square and neurology.塞缪尔·亚历山大·金尼尔·威尔逊。威尔逊氏病、女王广场与神经病学。
Rev Neurol (Paris). 2013 Dec;169(12):927-35. doi: 10.1016/j.neurol.2013.04.006. Epub 2013 Oct 11.
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MRI measurements predict PSP in unclassifiable parkinsonisms: a cohort study.MRI 测量可预测无法分类的帕金森病中的 PSP:一项队列研究。
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Do MRI features distinguish Wilson's disease from other early onset extrapyramidal disorders? An analysis of 100 cases.磁共振成像特征能否区分肝豆状核变性与其他早发性锥体外系疾病?100 例分析。
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威尔逊病中的脑桥中脑萎缩与姿势性不稳

Pontomesencephalic Atrophy and Postural Instability in Wilson Disease.

作者信息

Kalita J, Naik S, Bhoi S K, Misra U K, Ranjan A, Kumar S

机构信息

From the Departments of Neurology (J.K., S.K.B., U.K.M., A.R.)

Radiology (S.N., S.K.), Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India.

出版信息

AJNR Am J Neuroradiol. 2017 Jul;38(7):1343-1347. doi: 10.3174/ajnr.A5207. Epub 2017 May 11.

DOI:10.3174/ajnr.A5207
PMID:28495941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7959919/
Abstract

BACKGROUND AND PURPOSE

The MR Parkinsonism index helps in differentiating progressive supranuclear palsy from Parkinson disease and multisystem atrophy. Pontomesencephalic involvement is common in neurologic Wilson disease, but there is no prior study evaluating the MR Parkinsonism index and its indices in Wilson disease. We report the MR Parkinsonism index and its indices in Wilson disease and correlate these changes with clinical severity and postural reflex.

MATERIALS AND METHODS

Thirteen individuals with neurologic Wilson disease were included, and their clinical details, including neurologic severity, postural reflex abnormality, and location of signal changes on MR imaging, were noted. The 3D BRAVO T1 sequence was used for measurement of the MR Parkinsonism index and its indices. The MR Parkinsonism index and its indices were also obtained in 6 age- and sex-matched controls. The morphometric parameters in Wilson disease were compared with those in with healthy controls and among the patients with and without abnormal postural reflex.

RESULTS

The midbrain area was reduced in patients with Wilson disease compared with controls (112.08 ± 27.94 versus 171.95 ± 23.66 mm, = .002). The patients with an abnormal postural reflex had an increased MR Parkinsonism index and pons-to-midbrain ratio compared with controls, whereas these parameters were equivalent in patients with normal postural reflex and controls. The patients with abnormal postural reflex had more severe illness, evidenced by higher Burke-Fahn-Marsden scores (51.0 ± 32.27 versus 13.75 ± 12.37, = .04) and neurologic severity grades (2.57 ± 0.53 versus 1.67 ± 0.82, = .04).

CONCLUSIONS

An increase in the MR Parkinsonism index in Wilson disease is mainly due to midbrain atrophy and it correlates with neurologic severity and abnormal postural reflex.

摘要

背景与目的

磁共振帕金森病指数有助于鉴别进行性核上性麻痹与帕金森病及多系统萎缩。脑桥中脑受累在神经型威尔逊病中很常见,但此前尚无研究评估威尔逊病中的磁共振帕金森病指数及其各项指标。我们报告了威尔逊病中的磁共振帕金森病指数及其各项指标,并将这些变化与临床严重程度和姿势反射相关联。

材料与方法

纳入13例神经型威尔逊病患者,记录其临床细节,包括神经严重程度、姿势反射异常情况以及磁共振成像上信号改变的位置。采用3D BRAVO T1序列测量磁共振帕金森病指数及其各项指标。还选取了6名年龄和性别匹配的对照者测量磁共振帕金森病指数及其各项指标。比较了威尔逊病患者与健康对照者的形态学参数,以及有和无异常姿势反射的患者之间的形态学参数。

结果

与对照组相比,威尔逊病患者的中脑面积减小(112.08±27.94对171.95±23.66mm²,P = 0.002)。与对照组相比,有异常姿势反射的患者磁共振帕金森病指数和脑桥与中脑比值增加,而姿势反射正常的患者与对照组的这些参数相当。有异常姿势反射的患者病情更严重,表现为伯克 - 法恩 - 马斯登评分更高(51.0±32.27对13.75±12.37,P = 0.04)和神经严重程度分级更高(2.57±0.53对1.67±0.82,P = 0.04)。

结论

威尔逊病中磁共振帕金森病指数升高主要是由于中脑萎缩,且与神经严重程度和异常姿势反射相关。