Felig D M, Brusilow S W, Boyer J L
Department of Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
Gastroenterology. 1995 Jul;109(1):282-4. doi: 10.1016/0016-5085(95)90295-3.
Ornithine transcarbamylase deficiency is an X-linked disorder of the urea cycle that can cause hyperammonemic encephalopathy in hemizygous males and heterozygous females. Affected females typically limit protein intake in their diet. This case report describes a 36-year-old woman with ulcerative colitis who went into hyperammonemic coma after administration of total parenteral nutrition. A similar episode of coma had occurred 7 years earlier after she delivered a normal boy. Heterozygous ornithine transcarbamylase deficiency was diagnosed based on a positive allopurinol tolerance test result after elevated levels of plasma glutamine and low plasma citrulline were detected. The protein load associated with parenteral alimentation resulted in symptomatic expression of this partial enzyme deficiency in this unique case. Partial ornithine transcarbamylase deficiency must always be considered in adult women and men with hyperammonemia who have normal liver function test results.
鸟氨酸转氨甲酰酶缺乏症是一种尿素循环的X连锁疾病,可导致半合子男性和杂合子女性发生高氨血症性脑病。受影响的女性通常会限制饮食中的蛋白质摄入量。本病例报告描述了一名36岁患有溃疡性结肠炎的女性,在接受全胃肠外营养后陷入高氨血症昏迷。7年前她生下一个正常男孩后也曾发生过类似的昏迷发作。在检测到血浆谷氨酰胺水平升高和血浆瓜氨酸水平降低后,根据别嘌呤醇耐受性试验结果呈阳性,诊断为杂合子鸟氨酸转氨甲酰酶缺乏症。在这个独特的病例中,与胃肠外营养相关的蛋白质负荷导致了这种部分酶缺乏的症状性表现。对于肝功能检查结果正常但患有高氨血症的成年女性和男性,必须始终考虑到部分鸟氨酸转氨甲酰酶缺乏症。