Literature DB >> 729890

Study of enzyme defect in a case of ornithine transcarbamylase deficiency.

I A Qureshi, J Letarte, R Quellet.   

Abstract

Activity of liver ornithine transcarbamylase was measured in a biopsy obtained from a seven years old girl, suffering from chronic hyperammonemia and orotic aciduria. The activity of the defective enzyme was only 17% of that of a control. pH optimum was 8.1 in the patient and the control. However, the pH curves were different between 7.0 and 8.1. Km (ornithine) of the patient's ornithine transcarbamylase was within the normal range (0.41 nM), but the Km (carbamyl phosphate) was low (0.18 mM). The girl seems to be a heterozygote carrier of ornithine transcarbamylase deficiency due to an abnormal liver enzyme.

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Year:  1978        PMID: 729890

Source DB:  PubMed          Journal:  Diabete Metab        ISSN: 0338-1684


  3 in total

1.  Kinetic abnormalities of carbamyl phosphate synthetase-I in a case of congenital hyperammonaemia.

Authors:  I A Qureshi; J Letarte; R Ouellet; B Lemieux; L Cathelineau
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

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

Authors:  U Wendel; J Wieland; H J Bremer; C Bachmann
Journal:  Eur J Pediatr       Date:  1989-01       Impact factor: 3.183

3.  Regional amino acid neurotransmitter changes in brains of spf/Y mice with congenital ornithine transcarbamylase deficiency.

Authors:  L Ratnakumari; I A Qureshi; R F Butterworth
Journal:  Metab Brain Dis       Date:  1994-03       Impact factor: 3.584

  3 in total

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