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KCC3轴索性神经病:中枢和外周神经系统的神经病理学特征

KCC3 axonopathy: neuropathological features in the central and peripheral nervous system.

作者信息

Auer Roland N, Laganière Janet L, Robitaille Yves O, Richardson John, Dion Patrick A, Rouleau Guy A, Shekarabi Masoud

机构信息

Department of Pathology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University, Montréal, Québec, Canada.

出版信息

Mod Pathol. 2016 Sep;29(9):962-76. doi: 10.1038/modpathol.2016.90. Epub 2016 May 27.

Abstract

Hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum (HMSN/ACC) is an autosomal recessive disease of the central and peripheral nervous system that presents as early-onset polyneuropathy. Patients are hypotonic and areflexic from birth, with abnormal facial features and atrophic muscles. Progressive peripheral neuropathy eventually confines them to a wheelchair in the second decade of life, and death occurs by the fourth decade. We here define the neuropathologic features of the disease in autopsy tissues from eight cases. Both developmental and neurodegenerative features were found. Hypoplasia or absence of the major telencephalic commissures and a hypoplasia of corticospinal tracts to half the normal size, were the major neurodevelopmental defects we observed. Despite being a neurodegenerative disease, preservation of brain weight and a conspicuous absence of neuronal or glial cell death were signal features of this disease. Small tumor-like overgrowths of axons, termed axonomas, were found in the central and peripheral nervous system, indicating attempted axonal regeneration. We conclude that the neurodegenerative deficits in HMSN/ACC are primarily caused by an axonopathy superimposed upon abnormal development, affecting peripheral but also central nervous system axons, all ultimately because of a genetic defect in the axonal cotransporter KCC3.

摘要

与胼胝体发育不全相关的遗传性运动和感觉神经病(HMSN/ACC)是一种中枢和周围神经系统的常染色体隐性疾病,表现为早发性多发性神经病。患者从出生起就肌张力减退且无反射,面部特征异常,肌肉萎缩。进行性周围神经病最终使他们在20岁左右只能依靠轮椅行动,40岁左右死亡。我们在此定义了8例尸检组织中该疾病的神经病理学特征。发现了发育和神经退行性特征。我们观察到的主要神经发育缺陷是大脑主要连合发育不全或缺失,以及皮质脊髓束发育不全至正常大小的一半。尽管这是一种神经退行性疾病,但脑重量保持以及明显不存在神经元或神经胶质细胞死亡是该疾病的显著特征。在中枢和周围神经系统中发现了轴突的小肿瘤样过度生长,称为轴突瘤,表明存在轴突再生的尝试。我们得出结论,HMSN/ACC中的神经退行性缺陷主要是由叠加在异常发育之上的轴突病引起的,影响周围和中枢神经系统的轴突,所有这些最终都是由于轴突共转运体KCC3的基因缺陷。

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