Normal kynurenine metabolism in 2-oxoadipic aciduria

Journal of Inherited Metabolic Disease

Volumn 22, Issue 8, 1999, Pages 949-950

  Sewell, A C ^a,c   Herwig, J ^a   Bohles H ^a   Abeling, N G G M ^b   Van Gennip, A H ^b  

^a GOETHE UNIVERSITY   (Germany)

^b UNIVERSITY OF AMSTERDAM   (Netherlands)

^c UNIVERSITY HOSPITAL FRANKFURT   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADIPIC ACID DERIVATIVE; KYNURENINE;

ACIDURIA; AMINO ACID METABOLISM; ARTICLE; CASE REPORT; CLINICAL FEATURE; FEMALE; HUMAN; INFANT;

ADIPIC ACIDS; AMINO ACID METABOLISM, INBORN ERRORS; FEMALE; HUMANS; INFANT; KYNURENINE;

EID: 0032730616     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005672314435     Document Type: Article

References (4)

1. Chang YF, Cauley RK, Chang JD, et al (1997) L-Alpha-aminoadipate inhibits kynurenate synthesis in rat brain hippocampus and tissue culture. Neurochem Res 22: 825-829.
2. Goodman S, Frerman F (1995) Organic acidemias due to defects in lysine oxidation: 2-ketoadipic acidemia and glutaric acidemia. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1451-1460.
3. Jakobs C, de Grauw AJC (1992) A fatal case of 2-keto-, 2-hydroxy- and 2-aminoadipic aciduria: relation of organic aciduria to phenotype? J Inher Metab Dis 15: 279-280.
4. Wendel U, Rüdiger HW, Przyrembel H, Bremer HJ (1975) Alpha-ketoadipic aciduria: degradation studies with fibroblasts. Clin Chim Acta 58: 271-276.