甘油激酶缺乏症（GKD）是一种少见的X染色体隐性遗传性代谢缺陷病，可分为单纯型和复合型。
Glycerol kinase deficiency (GKD), a rare X-linked recessive disorder, is classified into two types: isolated and complex.
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.
近年来，脐血造血干细胞移植已广泛用于治疗儿童白血病、先天性免疫缺陷病、遗传性代谢病等方面。
Till now cord blood transplantation has been widely used in treating children leukemia, inborn immune deficiency, heritage metabolic disease and so on.
近年来，脐血造血干细胞移植已广泛用于治疗儿童白血病、先天性免疫缺陷病、遗传性代谢病等方面。
Till now cord blood transplantation has been widely used in treating children leukemia, inborn immune deficiency, heritage metabolic disease and so on.
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