Pregnancy and argininosuccinic aciduria

Journal of Inherited Metabolic Disease

Volumn 19, Issue 5, 1996, Pages 621-623

  Worthington, S ^a  

^a Western Sydney Genetics Program   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININOSUCCINATE LYASE; ARGININOSUCCINIC ACID;

ACIDURIA; ADULT; ARTICLE; CASE REPORT; ENZYME DEFICIENCY; FEMALE; FETUS MONITORING; FETUS OUTCOME; HUMAN; PERINATAL PERIOD; PREGNANCY; UREA CYCLE;

EID: 0029838454     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01799836     Document Type: Article

References (4)

1. Arn PH, Hauser ER, Thomas GH, Herman G, Hess D, Brusilow SW (1990) Hyperarnmonemia in women with a mutation at the ornithine carbamoyltransferase locus: a cause of postpartum coma. N Engl J Med 322: 1652-1655.
2. Brusilow SW, Horwich AL (1995) Urea cycle enzymes. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGrawHill, 1187-1232.
3. Lenke RL, Levy HL (1980) Maternal phenylketonuria and hyperphenylalaninaemia. An international survey of untreated and treated pregnancies. N Engl J Med 303: 1202-1208.
4. Maestri NE, Hauser ER, Bartholomew D, Brusilow SW (1991 ) Prospective treatment of urea cycle disorders. J Pediatr 119: 923-928.