Rapidly fatal hyperammonemic coma in adults. Urea cycle enzyme deficiency.
作者信息
Wilson B E, Hobbs W N, Newmark J J, Farrow S J
机构信息
Division of Endocrinology and Metabolism, University of Nevada School of Medicine, Las Vegas 89102.
出版信息
West J Med. 1994 Aug;161(2):166-8.
Abstract
摘要
相似文献
1
Rapidly fatal hyperammonemic coma in adults. Urea cycle enzyme deficiency.成人快速致死性高氨血症昏迷。尿素循环酶缺乏。
West J Med. 1994 Aug;161(2):166-8.
2
Urea cycle disorders in Thai infants: a report of 5 cases.泰国婴儿的尿素循环障碍：5例报告
J Med Assoc Thai. 2002 Aug;85 Suppl 2:S720-31.
3
Ornithine transcarbamylase deficiency: case report and review.鸟氨酸转氨甲酰酶缺乏症：病例报告与综述
Kans Med. 1995 Fall;96(3):135-8.
4
Plasma alpha-ketoglutarate in urea cycle enzymopathies and its role as a harbinger of hyperammonemic coma.尿素循环酶病中的血浆α-酮戊二酸及其作为高氨血症昏迷先兆的作用。
Pediatr Res. 1980 Dec;14(12):1316-9. doi: 10.1203/00006450-198012000-00008.
5
[Hyperammonemia type II as an example of urea cycle disorder].[以II型高氨血症为例的尿素循环障碍]
Wiad Lek. 2006;59(7-8):512-5.
6
Inborn errors of urea synthesis.尿素合成的先天性缺陷。
Ann Neurol. 1994 Feb;35(2):133-41. doi: 10.1002/ana.410350204.
7
Fatal clinical course of ornithine transcarbamylase deficiency in an adult heterozygous female patient.
Digestion. 1997;58(1):83-6. doi: 10.1159/000201428.
8
9
Fatal initial adult-onset presentation of urea cycle defect.尿素循环缺陷的致命性成人首发表现。
Arch Neurol. 2007 Dec;64(12):1777-9. doi: 10.1001/archneur.64.12.1777.
10
Risk of hyperammonemic coma in the puerperium: two cases of women with diagnosed and undiagnosed deficiency of urea cycle enzymes.产褥期高氨血症昏迷风险：两名诊断和未诊断的尿素循环酶缺陷女性病例。
Acta Obstet Gynecol Scand. 2010 Mar;89(3):404-6. doi: 10.3109/00016340903540646.
引用本文的文献
1
Hyperammonemic coma in a post-partum patient with undiagnosed urea cycle defect.一名患有未确诊尿素循环缺陷的产后患者出现高氨血症昏迷。
Indian J Crit Care Med. 2013 Mar;17(2):107-10. doi: 10.4103/0972-5229.114816.
本文引用的文献
1
Ornithine transcarbamylase deficiency presenting with strokelike episodes.表现为类中风发作的鸟氨酸转氨甲酰酶缺乏症。
J Pediatr. 1993 Mar;122(3):423-5. doi: 10.1016/s0022-3476(05)83432-8.
2
Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency.因氨甲酰磷酸合成酶I缺乏导致的产后昏迷和死亡。
Ann Intern Med. 1994 Feb 1;120(3):216-7. doi: 10.7326/0003-4819-120-3-199402010-00007.
3
Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis.尿素合成先天性代谢缺陷患儿发作性高氨血症的治疗
N Engl J Med. 1984 Jun 21;310(25):1630-4. doi: 10.1056/NEJM198406213102503.
4
Natural history of symptomatic partial ornithine transcarbamylase deficiency.有症状的部分鸟氨酸转氨甲酰酶缺乏症的自然病史。
N Engl J Med. 1986 Feb 27;314(9):541-7. doi: 10.1056/NEJM198602273140903.
5
Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency.
J Pediatr. 1986 Feb;108(2):236-41. doi: 10.1016/s0022-3476(86)80989-1.
6
Ornithine transcarbamylase deficiency: adult onset of severe symptoms.
Ann Intern Med. 1987 Apr;106(4):556-8. doi: 10.7326/0003-4819-106-4-556.
7
Ornithine transcarbamylase deficiency--a cause of bizarre behavior in a man.
N Engl J Med. 1986 Sep 18;315(12):744-7. doi: 10.1056/NEJM198609183151207.
8
Transient visual loss in ornithine transcarbamoylase deficiency.鸟氨酸转氨甲酰酶缺乏症中的短暂性视力丧失。
Am J Ophthalmol. 1987 Oct 15;104(4):407-12. doi: 10.1016/0002-9394(87)90232-7.
9
Computerized tomography in primary hyperammonemia.原发性高氨血症的计算机断层扫描
Neuroradiology. 1989;31(4):356-7. doi: 10.1007/BF00344184.
10
Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma.鸟氨酸氨甲酰基转移酶基因座突变女性的高氨血症。产后昏迷的一个原因。
N Engl J Med. 1990 Jun 7;322(23):1652-5. doi: 10.1056/NEJM199006073222307.
Zotero 插件