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Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentration.

作者信息

Wendel U, Wieland J, Bremer H J, Bachmann C

机构信息

Universitäts-Kinderklinik, Düsseldorf, Federal Republic of Germany.

出版信息

Eur J Pediatr. 1989 Jan;148(4):349-52. doi: 10.1007/BF00444132.

DOI:10.1007/BF00444132
PMID:2707281
Abstract

In a male with a partial defect of ornithine transcarbamylase (OTC) we observed that maintenance of arginine supply was crucial for adequate metabolic control in conjunction with a low protein diet. The arginine supplement had to be given such that the concentrations of arginine and ornithine in plasma were above 50 mumol/l. It appears that arginine is needed not only as an essential amino acid for protein synthesis but also as a precursor of ornithine. In this patient the substitution thus aimed at increasing the intramitochondrial ornithine in order to reach a critical substrate concentration for the kinetically abnormal OTC.

摘要

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引用本文的文献

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Diagnosis and management of inborn errors of metabolism.先天性代谢缺陷的诊断与管理
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本文引用的文献

1
Determination of orotic acid in children's urine.儿童尿液中乳清酸的测定。
J Clin Chem Clin Biochem. 1980 May;18(5):293-5. doi: 10.1515/cclm.1980.18.5.293.
2
Ornithine transcarbamylase deficiency in a boy with normal development.
J Pediatr. 1980 Mar;96(3 Pt 1):441-3. doi: 10.1016/s0022-3476(80)80694-9.
3
Effect of long-term administration of sodium benzoate to a patient with partial ornithine carbamoyl transferase deficiency.长期给一名部分鸟氨酸氨甲酰基转移酶缺乏患者服用苯甲酸钠的效果。
Clin Pediatr (Phila). 1983 Mar;22(3):206-8. doi: 10.1177/000992288302200309.
4
Ornithine carbamoyltransferase deficiency in an adult male patient: significance of hepatic ultrastructure in clinical diagnosis.
Pediatrics. 1983 Feb;71(2):224-32.
5
Immunochemical assay in 16 boys with ornithine transcarbamylase deficiency.
Adv Exp Med Biol. 1982;153:53-62. doi: 10.1007/978-1-4757-6903-6_8.
6
Arginine-responsive asymptomatic hyperammonemia in the premature infant.
J Pediatr. 1984 Jul;105(1):86-91. doi: 10.1016/s0022-3476(84)80369-8.
7
Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.精氨酸,对于尿素合成先天性代谢缺陷患者而言是一种必需氨基酸。
J Clin Invest. 1984 Dec;74(6):2144-8. doi: 10.1172/JCI111640.
8
Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.高氨血症。肝脏鸟氨酸转氨甲酰酶缺乏的一种变异类型。
Arch Dis Child. 1969 Apr;44(234):162-9. doi: 10.1136/adc.44.234.162.
9
Endogenous renal transport of free amino acids in infancy and childhood.婴儿期和儿童期内源性游离氨基酸的肾脏转运
Pediatrics. 1968 Sep;42(3):395-404.
10
Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant.部分鸟氨酸氨甲酰基转移酶缺乏症:一种尿素循环的先天性代谢缺陷,在一名男婴中表现为乳清酸尿症。
Can Med Assoc J. 1972 Sep 9;107(5):405-8.