Suppr超能文献

丙酮酸脱氢酶复合物缺乏症作为亚急性坏死性脑病( Leigh 病)的病因

Pyruvate dehydrogenase complex deficiency as a cause of subacute necrotizing encephalopathy (Leigh disease).

作者信息

Kretzschmar H A, DeArmond S J, Koch T K, Patel M S, Newth C J, Schmidt K A, Packman S

出版信息

Pediatrics. 1987 Mar;79(3):370-3.

PMID:3103091
Abstract

Leigh disease is a disorder with great clinical variability and for which diverse biochemical causes have been proposed. Clarification requires rigorous correlation of biochemical abnormalities with strict morphologic diagnosis; such an unambiguous association is the subject of this report. A patient with well-documented clinical and biochemical pyruvate dehydrogenase complex deficiency is shown on postmortem examination to have the specific CNS pathology of Leigh disease. These findings, considered together with the aggregate data in the literature, suggest strongly that pyruvate dehydrogenase complex deficiency is the basic defect in a subgroup of patients with Leigh disease.

摘要

Leigh病是一种临床变异性很大的疾病,针对其病因已提出了多种不同的生化机制。要明确病因,需要将生化异常与严格的形态学诊断进行严谨的关联分析;本报告的主题就是这种明确的关联。一名临床和生化检查充分证实患有丙酮酸脱氢酶复合物缺乏症的患者,尸检显示具有Leigh病特有的中枢神经系统病理学特征。结合文献中的总体数据来看,这些发现强烈提示丙酮酸脱氢酶复合物缺乏症是Leigh病患者亚组中的基本缺陷。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验