Carnitine acylcarnitine translocase deficiency Carnitine-acylcarnitine translocase (CACT) deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without food (fasting)
Carnitine-Acylcarnitine Translocase Deficiency | Newborn Screening Carnitine-acylcarnitine translocase (CACT) deficiency is an inherited (genetic) condition that prevents the body from breaking down certain fats and turning them into energy CACT is a protein in your body that helps with the processing of a type of fat called long-chain fatty acids
Carnitine-acylcarnitine translocase deficiency - MedlinePlus Mutations in the SLC25A20 gene cause CACT deficiency This gene provides instructions for making a protein called carnitine-acylcarnitine translocase (CACT) This protein is essential for fatty acid oxidation, a multistep process that breaks down (metabolizes) fats and converts them into energy
Carnitine-Acylcarnitine Translocase Deficiency Carnitine-acylcarnitine translocase deficiency (CACT deficiency) is a rare genetic condition that prevents the body from using certain fats (specifically long-chain fats) for energy
Carnitine-Acylcarnitine Translocase (CACT) Deficiency What is CACT Deficiency? Carnitine acylcarnitine translocase (CACT) deficiency is a rare inherited fatty acid oxidation disorder that occurs when the protein that transfers fats into the mitochondria is defective Mitochondria are the site within cells where energy is generated
Carnitine-acylcarnitine translocase - Wikipedia Carnitine-acylcarnitine translocase (CACT) is responsible for passive transport of carnitine and carnitine - fatty acid complexes and across the inner mitochondrial membrane as part of the carnitine shuttle system
Carnitine-Acylcarnitine Translocase Deficiency - an overview . . . Carnitine acylcarnitine translocase (CACT) transports fatty acids conjugated to carnitine across the mitochondrial membrane; CACT deficiency is one of the more severe FAODs, and the most common presentation is ventricular dysrhythmia and sudden neonatal death
Carnitine-Acylcarnitine Translocase Deficiency Disorder Carnitine-Acylcarnitine Translocase (CACT) Deficiency Disorder is a disorder that prevents the body from converting certain fats called long-chain fatty acids into energy, particularly during periods without food (fasting)