Case Reports Anales espanoles de pediatria. 1978 Mar;11(3):247-52.

[Subacute necrotizing encephalomielopathy. Leigh syndrome (author's transl)]

亚急性坏死性脑脊髓病（莱格氏病）翻译改进

Article in Spanish

J Felipe González, F Vargas Torcal, C Loris Pablo, F Borderas

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PMID: 666130

A 6-month-old girl with familiar history of two dead sisters few months old, was admitted to the Hospital with a neurological process. After her admission progressively worsened until her death. The patient had clinical manifestation of proximal tubular acidosis. Levels of lactic and piruvic acid were normal. Necropsic study was compatible with the diagnoses of subacute necrotizing encephalomielopathy of Leigh syndrome.

Keywords：leigh syndrome

关键词：亚急性坏死性脑脊髓病; 莱氏综合征

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[Subacute necrotizing encephalomielopathy. Leigh syndrome (author's transl)]

亚急性坏死性脑脊髓病（莱格氏病）翻译改进

Adult-onset Leigh Syndrome with a m.9176T>C Mutation Manifested As Reversible Cerebral Vasoconstriction Syndrome

成人型Leigh综合征中的一种m.9176T＞C突变以可逆性脑血管收缩综合征形式表现

Mitochondrial DNA point mutation T9176C in Leigh syndrome

线粒体DNA点突变T9176C与莱格病的关系研究

[Subacute necrotizing encephalomyelopathy (Leigh syndrome)]

亚急性坏死性脑脊髓病(莱igh病)

Cerebral magnetic resonance imaging lesions in leigh syndrome are variegated

莱格氏症候群的脑部磁振造影病灶变化多端

Novel mitochondrial C15620A variant may modulate the phenotype of mitochondrial G11778A mutation in a Chinese family with Leigh syndrome

线粒体C15620A新变异可能调节中国LHON家系中G11778A突变的表型效应

Ophthalmological manifestations in patients with Leigh syndrome

莱igh综合征患者的眼部表现

Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant

莱伯遗传性视神经病变m.11778G>A变种背景下双基因Leigh综合征

EPI-743 reverses the progression of the pediatric mitochondrial disease--genetically defined Leigh Syndrome

EPI-743 可逆转儿科线粒体遗传病利克氏症候群的发展进程

[Subacute necrotizing encephalomielopathy. Leigh syndrome (author's transl)]

亚急性坏死性脑脊髓病（莱格氏病） 翻译改进

Adult-onset Leigh Syndrome with a m.9176T>C Mutation Manifested As Reversible Cerebral Vasoconstriction Syndrome

成人型Leigh综合征中的一种m.9176T＞C突变以可逆性脑血管收缩综合征形式表现

Mitochondrial DNA point mutation T9176C in Leigh syndrome

线粒体DNA点突变T9176C与莱格病的关系研究

[Subacute necrotizing encephalomyelopathy (Leigh syndrome)]

亚急性坏死性脑脊髓病(莱igh病)

Cerebral magnetic resonance imaging lesions in leigh syndrome are variegated

莱格氏症候群的脑部磁振造影病灶变化多端

Novel mitochondrial C15620A variant may modulate the phenotype of mitochondrial G11778A mutation in a Chinese family with Leigh syndrome

线粒体C15620A新变异可能调节中国LHON家系中G11778A突变的表型效应

Ophthalmological manifestations in patients with Leigh syndrome

莱igh综合征患者的眼部表现

Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant

莱伯遗传性视神经病变m.11778G>A变种背景下双基因Leigh综合征

EPI-743 reverses the progression of the pediatric mitochondrial disease--genetically defined Leigh Syndrome

EPI-743 可逆转儿科线粒体遗传病利克氏症候群的发展进程

亚急性坏死性脑脊髓病（莱格氏病）翻译改进