Short-chain acyl-coenzyme A dehydrogenase deficiency
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Short-chain acyl-coenzyme A dehydrogenase deficiency (SCADD) is an autosomal recessive[6] fatty acid oxidation disorder which affects enzymes required to break down a certain group of fats called short chain fatty acids.[medical citation needed]
Quick Facts Other names, Symptoms ...
Short-chain acyl-coenzyme A dehydrogenase deficiency | |
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Other names | ACADS deficiency and SCAD deficiency,[1] |
Short-chain acyl-coenzyme A dehydrogenase deficiency has an autosomal recessive pattern of inheritance. | |
Symptoms | Cardiomyopathy , delayed speech[2] |
Causes | Mutations in the ACADS gene [3] |
Diagnostic method | Urine test, Genetic test[4][5] |
Treatment | Intravenous fluids/ high dextrose concentration [5] |
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