线粒体脑肌病

线粒体脑肌病是一种由线粒体代谢缺陷脱引起的脑肌病,属于线粒体疾病。此病由Luft于1962年首次采用改良戈莫理氏染色法(Gömöri trichrome stain,MGT)发现。[1]活体检查中,患者肌肉组织中带有破碎红纤维(或不整红边纤维,raggedredfiber,RRF)。这种线粒体疾病也可同时累及中枢神经系统引起多种线粒体肌病

线粒体脑肌病
类型线粒体肌病脑病变
分类和外部资源
医学专科神经学、​风湿病学、​内分泌学
ICD-9-CM277.87
MeSHD017237
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分型

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线粒体肌病根据临床不同综合征可分为几类:[2][3]

参考文献

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  1. ^ Rolf Luft, Denis Ikkos, Genaro Palmieri, Lars Ernster, and Björn Afzelius. A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study. Journal of Clinical Investigation. Sep 1962, 41 (9): 1776–1804. PMID 14467237. doi:10.1172/JCI104637 (英语). [永久失效链接]
  2. ^ Melone MA, Tessa A, Petrini S, Lus G, Sampaolo S, di Fede G, Santorelli FM, Cotrufo R. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype. Archives of Neurology. Feb 2004, 61 (2): 269–272. PMID 14967777. doi:10.1001/archneur.61.2.269 (英语). [永久失效链接]
  3. ^ Naini AB, Lu J, Kaufmann P, Bernstein RA, Mancuso M, Bonilla E, Hirano M, DiMauro S. Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF. Archives of Neurology. Mar 2005, 62 (3): 473–476. PMID 15767514. doi:10.1001/archneur.62.3.473 (英语). [永久失效链接]
  4. ^ D Crimmins, J G Morris, G L Walker, C M Sue, E Byrne, S Stevens, B Jean-Francis, C Yiannikas, and R Pamphlett. Mitochondrial encephalomyopathy: variable clinical expression within a single kindred. Journal of Neurology, Neurosurgery & Psychiatry. Aug 1993, 56 (8): 900–905. PMC 1015147 . PMID 8350109. doi:10.1136/jnnp.56.8.900 (英语). 

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