Abstract
Disorders of fatty acid metabolism are known to be responsible for cases of sudden and unexpected death in infancy. At least 14 disorders are known at present. 120 cases of sudden infant death syndrome (SIDS) had been examined for a prevalent mutation (G985) causing medium chain acyl CoA dehydrogenase deficiency, which is inherited in an autosomal recessive mode. No over-representation of either homozygous or heterozygous cases was found.
Original language | English |
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Journal | Journal of Clinical Pathology |
Volume | 50 |
Issue number | 4 |
Pages (from-to) | 212-7 |
Number of pages | 6 |
ISSN | 1366-8714 |
Publication status | Published - Aug 1997 |
Keywords
- Acyl-CoA Dehydrogenase
- Acyl-CoA Dehydrogenases
- Cell Culture Techniques
- Child, Preschool
- Fatty Acids
- Female
- Fibroblasts
- Heterozygote
- Humans
- Infant
- Infant, Newborn
- Lipid Metabolism, Inborn Errors
- Male
- Oxidation-Reduction
- Point Mutation
- Prospective Studies
- Sudden Infant Death