Retrospective diagnosis of 3-hydroxydicarboxylic aciduria by analysis of filter paper blood samples
- 1 March 1990
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 13 (2) , 165-168
- https://doi.org/10.1007/bf01799680
Abstract
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.Keywords
This publication has 3 references indexed in Scilit:
- 3-hydroxydicarboxylic aciduria—a fatty acid oxidation defect with severe prognosisThe Journal of Pediatrics, 1990
- The inborn errors of mitochondrial fatty acid oxidationJournal of Inherited Metabolic Disease, 1987
- EVALUATION OF A NATION‐WIDE NEONATAL METABOLIC SCREENING PROGRAMME IN SWEDEN 1965–1979Acta Paediatrica, 1981