Mitochondrial membrane protein-associated neurodegeneration presenting with pure motor neuropathy: A rare case report and review of the literature

Q3 Medicine Annals of Movement Disorders Pub Date : 2024-06-03 DOI:10.4103/aomd.aomd_3_24
Vikas Lakhanpal, S. Peer, Ramandeep Singh, Bhawna Sharma
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引用次数: 0

Abstract

Neurodegeneration with brain iron accumulation is a collective term for neurodegenerative disorders characterized by excessive deposition of iron in the brain, especially in the globus pallidus and substantia nigra. Mitochondrial membrane protein-associated neurodegeneration mainly affects the pyramidal and extrapyramidal systems, and patients can present with various manifestations during disease progression, including gait disorder, dystonia, ataxia, swallowing dysfunction, neuropsychiatric abnormalities, cognitive disabilities, optic atrophy, and, sometimes, peripheral neuropathy. We report a patient of mitochondrial membrane protein-associated neurodegeneration with peripheral neuropathy as the predominant symptom.
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线粒体膜蛋白相关神经变性伴有单纯运动神经病变:罕见病例报告和文献综述
脑铁积聚性神经退行性病变是一种神经退行性疾病的统称,其特征是脑内铁过度沉积,尤其是在苍白球和黑质。线粒体膜蛋白相关神经退行性病变主要影响锥体和锥体外系,患者在疾病进展过程中会出现各种表现,包括步态障碍、肌张力障碍、共济失调、吞咽功能障碍、神经精神异常、认知障碍、视神经萎缩,有时还会出现周围神经病变。我们报告了一名以周围神经病变为主要症状的线粒体膜蛋白相关神经变性患者。
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来源期刊
Annals of Movement Disorders
Annals of Movement Disorders Medicine-Surgery
CiteScore
0.60
自引率
0.00%
发文量
0
审稿时长
17 weeks
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