Literature DB >> 197778

Carbamyl-phosphate-synthetase deficiency with neonatal onset of symptoms.

J P Farriaux, C Ponte, R J Pollitt, P Lequien, P Formstecher, J L Dhondt.   

Abstract

The clinical course and biochemical findings in a case of carbamyl-phosphate-synthetase deficiency are described. The patient, a boy, presented 48 h after birth with rapidly developing hypotonia and hypothermia. Pulmonary haemorrhage, melaena and haematemesis ensued and despite ventilatory assistance and peritoneal dialysis the patient died on the fifth day. A virtual absence of carbamyl phosphate synthetase I (N-acetylglutamate dependent) was proved by analysis of tissue samples removed post mortem. Other urea cycle enzymes were normal.

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Year:  1977        PMID: 197778     DOI: 10.1111/j.1651-2227.1977.tb07940.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  3 in total

1.  Detection of carbamyl phosphate synthetase 1 deficiency using duodenal biopsy samples.

Authors:  J P Farriaux; J L Dhondt; R J Pollitt
Journal:  Arch Dis Child       Date:  1980-10       Impact factor: 3.791

2.  Carbamyl phosphate synthetase deficiency with lethal neonatal outcome.

Authors:  J Jaeken; H Devlieger; C Bachmann; J Van Aerde; L Corbeel; E Eggermont
Journal:  Eur J Pediatr       Date:  1982-09       Impact factor: 3.183

3.  Autosomal recessive inheritance of human mitochondrial carbamyl phosphate synthetase deficiency.

Authors:  J W McReynolds; B Crowley; M J Mahoney; L E Rosenberg
Journal:  Am J Hum Genet       Date:  1981-05       Impact factor: 11.025

  3 in total

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