这是诊断甲基丙二酸尿症的重要方法。
This is a very important method in diagnosing methylmalonic aciduria.
目的探讨甲基丙二酸血症(MMA)的临床特征和治疗方法。
Objective Methylmalonic acidemia (MMA) is one of the most common disorders of congenital organic acid metabolism.
甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
Methylmalonic acidemia is an inherited metabolic disorder, which is caused by deficiency of methylmalonyl-coenzyme a mutase or its cofactor adenosylcobalamin.
它们是乙酸、苯甲醛、正葵酸、14-甲基十五烷酸甲酯、丙三醇、苯甲酸、6 ，9-十八碳二烯酸甲酯、角鲨烷、硬脂酸和二十烷基油酸酯。
They were acetic acid, benzaldehyde, n caproic acid, 14 methyl pentadecanoic methyl ester, glycerin, benzoic acid, 6,9 octadecadienoic methyl ester, squalane, stearic acid and oleic eicosyl ester.
它们是乙酸、苯甲醛、正葵酸、14-甲基十五烷酸甲酯、丙三醇、苯甲酸、6 ，9-十八碳二烯酸甲酯、角鲨烷、硬脂酸和二十烷基油酸酯。
They were acetic acid, benzaldehyde, n caproic acid, 14 methyl pentadecanoic methyl ester, glycerin, benzoic acid, 6,9 octadecadienoic methyl ester, squalane, stearic acid and oleic eicosyl ester.
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