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