Winokur P A, Vashistha K, Seshamani R
Pediatrics. 1978 Jun;61(6):902-3.
Aminoacidopathies are rare metabolic defects that frequently present shortly after birth or in early infancy with vomiting, dehydration, ketoacidosis, and a peculiar body odor. If not recognized early, these can result in developmental retardation and/or death. A case of isovalericacidemia is reported to emphasize the importance of metabolic screening when an infant presents with the above-mentioned symptoms along with an anion gap greater than 20 mEq/liter. In our patient, a metabolic disorder was suggested by the clinical presentation and was confirmed by measuring elevated levels of biproducts. The infant was given a low-leucine diet and has developed normally since then.
氨基酸病是罕见的代谢缺陷,常在出生后不久或婴儿早期出现呕吐、脱水、酮症酸中毒和特殊体味。如果不及早识别,这些情况可导致发育迟缓及/或死亡。本文报告了一例异戊酸血症病例,以强调当婴儿出现上述症状且阴离子间隙大于20毫当量/升时进行代谢筛查的重要性。在我们的患者中,临床表现提示存在代谢紊乱,通过测量代谢产物水平升高得以证实。该婴儿接受了低亮氨酸饮食,此后发育正常。