Article PDF
Avoid common mistakes on your manuscript.
References
Bennett MJ, Sherwood WG, Gibson KM, Burlina AB (1993) Secondary inhibition of multiple NAD-requiring dehydrogenases in respiratory chain complex I deficiency: possible metabolic markers for the primary defect.J Inher Metab Dis 16: 560–562.
Bergoffen J, Kaplan P, Hale DE, Bennett MJ, Berry GT (1993) Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chainl-3-hydroxyacyl-CoA dehydrogenase deficiency.J Inher Metab Dis 16: 851–856.
Carpenter K, Pollitt RJ, Middleton B (1992) Human liver long-chain 3-hydroxyacyl-coenzyme-A dehydrogenase is a multifunctional membrane-bound beta oxidation enzyme of mitochondria.Biochem Biophys Res Commun 183: 443–448.
Christensen E, Brandt NJ, Schmalbruch H, Kamieniecka Z, Hertz B, Ruitenbeek W (1993) Muscle cytochromec oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl-CoA dehydrogenase deficiency.J Inher Metab Dis 16: 553–556.
Hagenfeldt L, Wibom R, Venizelos N, von Dobeln U (1992) Oxidation of fatty acids in fibroblasts from patients with respiratory chain defects.Proc 30th Symposium SSIEM, P.136 (Abstract).
Hale DE, Thorpe C, Braat K et al (1990) Thel-3-hydroxyacyl-CoA dehydrogenase deficiency.Prog Clin Biol Res 321; 503–510.
Lehnert W, Ruitenbeek W (1993) Ethylmalonic aciduria associated with progressive neurological disease and partial cytochromec oxidase deficiency.J Inher Metab Dis 16: 557–559.
Manning NJ, Olpin SE, Pollitt RJ, Webley J (1990) Comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of fatty acid oxidation defects in intact cultured fibroblasts.J Inher Metab Dis 13: 58–68.
Olpin SE, Manning NJ, Carpenter K, Middleton B, Pollitt RJ (1992) Differential diagnosis of hydroxydicarboxylic aciduria based on release of3H2O from [9,10-3H]myristic and [9,10-3H]palmitic acids by intact cultured fibroblasts.J Inher Metab Dis 15: 883–890.
Pollitt RJ (1990) Clinical and biochemical presentation in 20 cases of hydroxydicarboxylic aciduria.Prog Clin Biol Res 321: 495–502.
Wanders RJA, Duran I, IJlst L et al (1989) Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.Lancet 1: 52–53.
Wanders RJA, IJlst L, van Gennip et al (1990) Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid β-oxidation.J Inher Metab Dis 13: 311–314.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Bennett, M.J., Weinberger, M.J., Sherwood, W.G. et al. Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. J Inherit Metab Dis 17, 283–286 (1994). https://doi.org/10.1007/BF00711808
Issue Date:
DOI: https://doi.org/10.1007/BF00711808