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| Multiple acyl-CoA dehydrogenase deficiency in a neonate |
| CHEN Jun-Cao, CHEN Ping-Yang |
| Division of Neonatology, Children’s Medical Center, Second Xiangya Hospital, Central South University, Changsha, 410011, China |
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| [1] | Sugai F, Baba K, Toyooka K, Liang W, Nishiol I, Yamadera M, et al. Adult-onset multiple acyl CoA dehydrogenation deficiency associated with an abnormal isoenzyme pattern of serum lactate dehydrogenase[J]. Neuromuscul Disord, 2012, 22(2): 159-161.
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| [2] | al-Essa MA, Hashed MS, Bakheet SM, Patay ZJ, Ozand PT. Glutaric aciduria type II: observations in seven patients with neonatal-and late-onset disease[J]. Perinatol, 2000, 20(2): 120-128.
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| [3] | 鲍梦馨, 朱梅佳. 多种酰基辅酶A脱氢酶缺乏症两家系临床、病理及分子遗传学研究[D]. 山东大学硕士学位论文, 2012.
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| [4] | 章瑞南, 邱文娟, 叶军, 韩连书, 张惠文, 邱蕊, 等. 多种酰基辅酶A 脱氢酶缺乏症儿童与成人患者临床特点比较[J]. 临床儿科杂志, 2012, 30(5): 446-449.
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