Mitochondrial neuropathy and neurogenic features in mitochondrial myopathy

被引:10
作者
Lu, Jian-Qiang [1 ]
Tarnopolsky, Mark A. [2 ,3 ]
机构
[1] McMaster Univ, Dept Pathol & Mol Med Neuropathol, Hamilton, ON, Canada
[2] McMaster Univ, Dept Med Neurol, Hamilton, ON, Canada
[3] McMaster Univ, Dept Pediat, Hamilton, ON, Canada
关键词
Mitochondrial disease; Mitochondrial myopathy; Mitochondrial neuropathy; Neuromuscular junction; Neurogenic features; Nerve and muscle pathology; PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; KEARNS-SAYRE SYNDROME; PERIPHERAL NEUROPATHY; NEUROMUSCULAR-JUNCTION; SKELETAL-MUSCLE; SPINOCEREBELLAR ATAXIA; INFANTILE ONSET; POINT MUTATION; LEIGH-SYNDROME; DNA;
D O I
10.1016/j.mito.2020.11.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial diseases (MIDs) involve multiple organs including peripheral nerves and skeletal muscle. Mitochondrial neuropathy (MN) and mitochondrial myopathy (MM) are commonly associated and linked at the neuromuscular junction (NMJ). Herein we review MN in connection with neurogenic features of MM, and pathological evidence for the involvement of the peripheral nerve and NMJ in MID patients traditionally assumed to have predominantly MM. MN is not uncommon, but still likely under-reported, and muscle biopsies of MM commonly exhibit neurogenic features. Pathological examination remains the gold standard to assess the nerve and muscle changes in patients with MIDs. Ultrastructural studies by electron microscopy are often necessary to fully characterize the pathology of mitochondrial cytopathy in MN and MM.
引用
收藏
页码:52 / 61
页数:10
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