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"Acyl-CoA" dehydrogenase deficiency
- Short/branched chain acyl-CoA dehydrogenase (SBCAD) deficiency (also known as 2-methylbutyryl-CoA dehydrogenase deficiency) is a rare disorder in which the body ...
- Short-chain acyl-CoA dehydrogenase (SCAD) deficiency is a condition that prevents the body from converting certain fats into energy, especially during periods ...
- Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a condition that prevents the body from converting certain fats into energy, particularly during ...
- ... deficiency MCAD deficiency MCADD MCADH deficiency Medium chain acyl-CoA dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Genetic ...
- ... chain, deficiency LCHAD deficiency Long-chain 3-hydroxy acyl CoA dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency ...
- ... 2 Glutaric aciduria, type 2 MAD MADD Multiple acyl-CoA dehydrogenase deficiency Multiple FAD dehydrogenase deficiency Genetic Testing Registry: Multiple ...
- ... not show signs and symptoms of the condition. Acyl-CoA dehydrogenase 9 deficiency Deficiency of acyl-CoA dehydrogenase family member 9 ... deficiency due to ACAD9 deficiency Genetic Testing Registry: Acyl-CoA dehydrogenase 9 deficiency Isolated complex I deficiency National Organization for Rare ...
- ... in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship. Hum ...
- ... in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship. Hum ...
- Newborn Screening (National Library of Medicine)Your newborn infant has screening tests before leaving the hospital. There may be different tests depending on the state where you live. They include: Tests ...
