CHEN Jun-Cao, CHEN Ping-Yang.
Multiple acyl-CoA dehydrogenase deficiency in a neonate[J]. Chinese Journal of Contemporary Pediatrics. 2013, 15(12): 1098-1099 https://doi.org/10.7499/j.issn.1008-8830.2013.12.015
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[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. [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. [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. [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.
PDF(992 KB)
