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Carnitine deficiency
- Primary carnitine deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without food (fasting). Carnitine, ...
- ... type I CPT I deficiency Liver form of carnitine palmitoyltransferase deficiency Genetic Testing Registry: Carnitine palmitoyl transferase 1A deficiency ...
- ... signs and symptoms of the condition. CACT deficiency Carnitine acylcarnitine translocase deficiency Carnitine-acylcarnitine carrier deficiency Genetic Testing Registry: Carnitine ...
- ... not show signs and symptoms of the condition. Carnitine palmitoyltransferase 2 deficiency CPT II deficiency CPT2 deficiency Genetic Testing Registry: ...
- ... SLC22A5 gene have been found to cause primary carnitine deficiency. Some of these variants create a premature stop ... lead to some of the features of primary carnitine deficiency, such as muscle weakness and hypoglycemia. Fatty acids ...
- 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 ...
- Lipid Metabolism Disorders (National Library of Medicine)Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
- Nonalcoholic Fatty Liver Disease (American Academy of Family Physicians)American Academy of Family Physicians ... Fatty Liver Disease/Learn More ... Fatty Liver Disease
- Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDFMuscular Dystrophy Association ... muscular dystrophy; exercise with a disability; neuromuscular disease; adapted exercise; accesible sports equipment; power ...
- Find a Neuromuscular Disease (Muscular Dystrophy Association)Muscular Dystrophy Association ... Neuromuscular Disorders/Start Here ... Neuromuscular Disorders ... MDA is the #1 health nonprofit advancing research, care and advocacy ...
