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Valproate-induced lethal hyperammonaemic coma in a carrier of ornithine carbamoyltransferase deficiency.

作者信息

Tokatli A, Coşkun T, Cataltepe S, Ozalp I

机构信息

Department of Metabolism, Hacettepe University, Ankara, Turkey.

出版信息

J Inherit Metab Dis. 1991;14(5):836-7. doi: 10.1007/BF01799961.

DOI:10.1007/BF01799961
PMID:1779634
Abstract
摘要

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1
Valproate-induced lethal hyperammonaemic coma in a carrier of ornithine carbamoyltransferase deficiency.
J Inherit Metab Dis. 1991;14(5):836-7. doi: 10.1007/BF01799961.
2
[Hyperammonaemic coma after valproate therapy as adult onset of ornithine transcarbamylase deficiency].[丙戊酸盐治疗后出现高氨血症性昏迷，为成人型鸟氨酸转氨甲酰酶缺乏症]
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3
Valproate as a cause of hyperammonemia in heterozygotes with ornithine-transcarbamylase deficiency.
Neurology. 1995 Mar;45(3 Pt 1):593-4. doi: 10.1212/wnl.45.3.593.
4
Heterozygote ornithine transcarbamylase deficiency presenting as symptomatic hyperammonemia during initiation of valproate therapy.杂合子鸟氨酸转氨甲酰酶缺乏症在丙戊酸治疗开始时表现为有症状的高氨血症。
Neurology. 1992 Mar;42(3 Pt 1):666-8. doi: 10.1212/wnl.42.3.666.
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Lethal hyperammonaemic coma due to ornithine transcarbamylase deficiency presenting as brain stem encephalitis in a previously asymptomatic ten-year-old boy.一名既往无症状的10岁男孩因鸟氨酸转氨甲酰酶缺乏症导致致命性高氨血症昏迷，表现为脑干脑炎。
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Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency.在未识别的鸟氨酸转氨甲酰酶缺乏症患者中，丙戊酸治疗开始后出现高氨血症性脑病。
J Neurol Neurosurg Psychiatry. 1998 May;64(5):680-2. doi: 10.1136/jnnp.64.5.680.
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Sodium valproate and ornithine carbamyl transferase deficiency.
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Proceedings: Case of hyperammonaemia due to ornithine transcarbamylase deficiency.会议记录：鸟氨酸转氨甲酰酶缺乏所致高氨血症病例
Arch Dis Child. 1974 Sep;49(9):747. doi: 10.1136/adc.49.9.747-a.
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Continuous venovenous haemofiltration in hyperammonaemic coma of an adult with non-diagnosed partial ornithine transcarbamylase deficiency.成人未确诊的部分鸟氨酸转氨甲酰酶缺乏症高氨血症昏迷患者的持续静静脉血液滤过
Nephrol Dial Transplant. 1999 May;14(5):1282-4. doi: 10.1093/ndt/14.5.1282.
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Hyperammonemic coma due to parenteral nutrition in a woman with heterozygous ornithine transcarbamylase deficiency.一名患有杂合性鸟氨酸转氨甲酰酶缺乏症的女性因肠外营养导致高氨血症昏迷。
Gastroenterology. 1995 Jul;109(1):282-4. doi: 10.1016/0016-5085(95)90295-3.

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Neurological implications of urea cycle disorders.尿素循环障碍的神经学影响。
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Effect of single oral dose of sodium benzoate on ureagenesis in healthy men and two patients with late onset citrullinaemia.单次口服苯甲酸钠对健康男性和两名迟发性瓜氨酸血症患者尿素生成的影响。
Eur J Clin Pharmacol. 1993;45(5):465-8. doi: 10.1007/BF00315519.
3
Neurological deterioration in patients with urea cycle disorders under valproate therapy--a cause for concern.

本文引用的文献

1
Hyperammonemia with valproic acid therapy.
J Pediatr. 1981 Aug;99(2):317-9. doi: 10.1016/s0022-3476(81)80489-1.
2
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.
3
Lethal hyperammonaemic coma due to ornithine transcarbamylase deficiency presenting as brain stem encephalitis in a previously asymptomatic ten-year-old boy.一名既往无症状的10岁男孩因鸟氨酸转氨甲酰酶缺乏症导致致命性高氨血症昏迷，表现为脑干脑炎。
J Inherit Metab Dis. 1987;10(3):271. doi: 10.1007/BF01800076.
Eur J Pediatr. 1995 Jul;154(7):593-4. doi: 10.1007/BF02074851.