Coude M M, Charpentier C, Bonnefont J P, Cheron G, Kamoun P
Laboratoire de Biochimie Médicale B, Hôpital Necker Enfants Malades, Paris, France.
J Inherit Metab Dis. 1991;14(5):668-73. doi: 10.1007/BF01799931.
Organic acids have been determined in aqueous humour and plasma by gas chromatography-mass spectrometry in 38 cases of infant death and 4 cases of inherited metabolic disease: one had a complex fatty-acid oxidation disorder with a large urinary excretion of adipic acid, the others had a disorder of propionate catabolism with a large urinary excretion of methylmalonic acid. In each case we found in aqueous humour the abnormal metabolite present in urine. Thus aqueous humour could be a suitable material for retrospective diagnosis of inherited metabolic diseases at autopsy in sudden infant death syndrome.
通过气相色谱-质谱联用技术,对38例婴儿死亡病例和4例遗传性代谢疾病病例的房水和血浆中的有机酸进行了测定。其中1例患有复杂的脂肪酸氧化障碍,尿中大量排泄己二酸;其他病例患有丙酸分解代谢障碍,尿中大量排泄甲基丙二酸。在每例病例中,我们在房水中均发现了尿液中存在的异常代谢物。因此,房水可能是在婴儿猝死综合征尸检时对遗传性代谢疾病进行回顾性诊断的合适材料。