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Lipid peroxidation in homocysteinaemia

descriptionPublicationkeyboard_double_arrow_right Article 01 May 1992 English Publisher:WileyJournal:Journal of Inherited Metabolic Disease, volume 15, pages 419-422 (issn: 0141-8955, eissn: 1573-2665,

Authors: R.A. de Abreu; Godfried H.J. Boers; Ad M. Stadhouders; D. P. E. Engelen; M. T. W. B. TePoele-Pothoff; J. M. F. Trijbels; Henk J. Blom; +1 Authors

doi: 10.1007/bf02435993

pmid: 1405484

Lipid peroxidation in homocysteinaemia

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Abstract

Homocysteinaemia due to cystathione synthase deficiency (CSD: McKusick 236200) is a rare autosomal recessive inborn error of methionine metabolism. The most life-threatening complications caused by CSD are thromboembolism and vascular abnormalities. Boers et al (1985) provided evidence that even mild homocysteinaemia, as seen in heterozygote CSD patients, is predisposing for development of premature peripheral and cerebral occlusive arterial disease

Related Organizations

Ege University
Turkey

Keywords

Adult, Spectrometry, Fluorescence, Malondialdehyde, Homozygote, Cystathionine beta-Synthase, Humans, Lipid Peroxidation, Homocysteine

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