Journal of Inherited Metabolic Disease · 2001 · 13 citations · 21 references
Life SciencesNutritionNutritional SciencesHuman NutritionLipid BiochemistryNutritional BiochemistryEnzyme DeficienciesEssential Fatty AcidsFatty Acid ChemistryFatty Acid MetabolismLipid MetabolismNutritional DeficienciesAcyl-coa Dehydrogenase RegulationAcyl-coa DehydrogenasesDietary Fatty Acid RequirementsDietary Fatty AcidsEssential Fatty Acid MetabolismFatty Acid Oxidation Enzyme DeficienciesPolyunsaturated Fatty Acid MetabolismUnsaturated Fatty Acids
Nutritional management of very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is based on the avoidance of fasting and substitution of medium-chain triglycerides for long- and very long-chain triglycerides. We report two cases of this disease, which developed omega-6 essential fatty acid deficiency after three and five months from the beginning of nutritional therapy (SHS product: Monogen). This alteration could be especially dangerous in these patients owing to their possible susceptibility to the development of pigmentary retinopathy. The incorporation of linoleic acid as 3-4% of total caloric intake supported as soybean oil ameliorates this deficiency. We wish to remark on this early complication in the nutritional management of VLCAD deficiency and the possibility of rescue by the incorporation of soybean oil into the diet.
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Anne Voss, Meri Reinhart, Shankar K. Sankarappa et al. · Journal of Biological Chemistry · 1991 · 664 citations · Full text