Summary
Five patients with 3-hydroxydicarboxylic aciduria have been investigated. Two of them had elder siblings who had died unexpectedly in early infancy. Stored filter paper blood samples obtained from the patients and their siblings for neonatal screening were retrieved. Elevated levels of 3-hydroxy fatty acids were observed in the samples from three of the five patients with 3-hydroxydicarboxylic aciduria and in the samples from both siblings.
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References
Alm, J. and Larsson, A. Evaluation of a nationwide neonatal metabolic screening program in Sweden 1965–1979.Acta Paediatr. Scand. 70 (1981) 601–607
Hagenfeldt, L., von Döbeln, U., Holme, E., Alm, J., Brandberg, G., Enocksson, E. and Lindeberg, L. 3-Hydroxy-dicarboxylic aciduria — a fatty acid oxidation defect with severe prognosis.J. Pediatr. (1989), in press
Vianey-Liaud, C., Divry, P., Gregersen, N. and Mathieu, M. The inborn errors of mitochondrial fatty acid oxidation.J. Inher. Metab. Dis. 10 Suppl. 1 (1987) 159–198
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von Döbeln, U., Venizelos, N. & Hagenfeldt, L. Retrospective diagnosis of 3-hydroxydicarboxylic aciduria by analysis of filter paper blood samples. J Inherit Metab Dis 13, 165–168 (1990). https://doi.org/10.1007/BF01799680
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DOI: https://doi.org/10.1007/BF01799680