Roth K, Cohn R, Yandrasitz J, Preti G, Dodd P, Segal S
J Pediatr. 1976 Feb;88(2):229-35. doi: 10.1016/s0022-3476(76)80987-0.
A patient is described in whom lactic acidosis of very severe degree was found to coincide with the presence of beta-methylcrotonic acid and rho-hydroxyphenyllactic acid in urine in large amounts, while beta-hydroxyisovaleric acid was found to be a relatively minor excretion product. Beta-methylcrotonic acid is demonstrated, for the first time, to be present in blood and CSF. These findings are discussed in relation to the patients previously reported to have beta-methylcrotonylglycinuria and raise the possibility that our patient's organic aciduria may be secondary to acquired disease rather than to an inborn error of metabolism.
本文描述了一名患者,该患者被发现存在非常严重的乳酸性酸中毒,同时尿液中大量存在β-甲基巴豆酸和ρ-羟基苯乳酸,而β-羟基异戊酸则是相对较少的排泄产物。首次证明β-甲基巴豆酸存在于血液和脑脊液中。结合之前报道的患有β-甲基巴豆酰甘氨酸尿症的患者对这些发现进行了讨论,并提出我们这位患者的有机酸尿症可能继发于后天疾病而非先天性代谢缺陷的可能性。