Aleck K A, Kaplan A M, Sherwood W G, Robinson B H
Department of Pediatrics, Phoenix Children's Hospital, AZ 85006.
Arch Neurol. 1988 Sep;45(9):987-9. doi: 10.1001/archneur.1988.00520330073012.
Pyruvate dehydrogenase deficiency is among the most common causes of congenital lactic acidosis. We describe siblings with congenital lactic acidosis due to a deficiency of pyruvate dehydrogenase complex. The findings of computed tomography and pathologic studies suggest that central nervous system damage had occurred in utero. These observations have implications for treatment and outcome in patients with enzymatic defects causing congenital lactic acidosis.
丙酮酸脱氢酶缺乏症是先天性乳酸性酸中毒最常见的病因之一。我们描述了因丙酮酸脱氢酶复合物缺乏而患有先天性乳酸性酸中毒的同胞。计算机断层扫描和病理研究结果表明,中枢神经系统损伤发生在子宫内。这些观察结果对因酶缺陷导致先天性乳酸性酸中毒患者的治疗和预后具有重要意义。