参予者的类型 新生儿出生体重小于2500公克，出生24小时内证实有代谢性酸血症（动脉血液气体分析）。
Types of participants Newborn infants with birth weight <2500g and less than 24 hours of age with proven metabolic acidaemia (on arterial blood gas).
这篇文献的主要目的是要评估对于低出生体重（<2500公克）新生儿的早期（在出生后24小时内）代谢性酸血症，在快速矫正后产生的短期及长期的效应。
The main objective was to assess the short and long-term effects of the rapid correction of early (first 24 hours) metabolic acidaemia in LBW (<2500g birth weight) neonates.
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.
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