Kretzschmar H A, DeArmond S J, Koch T K, Patel M S, Newth C J, Schmidt K A, Packman S
Pediatrics. 1987 Mar;79(3):370-3.
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.
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。