Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ-oxidation

July 7, 2017 | Autor: C. Jakobs | Categoría: Nursing, Pediatrics, Treatment Outcome, Mitochondria, Pediatric nursing, Adolescent, Liver diseases, High Frequency, Heart Failure, Pregnancy, Humans, Child, Liver Cirrhosis, Liver, Mutation, Female, Male, Hypoglycemia, Fatty Acid Oxidation, Infant, Follow-up studies, Netherlands, Differential Diagnosis, HELLP Syndrome, Phenotype, Clinical Sciences, Newborn Infant, L-carnitine, Questionnaires, Optometry and Ophthalmology, Public health systems and services research, Survival Rate, Fatty Acid, Health surveys, Multienzyme complexes, Cardiomyopathies, Status Epilepticus, Base Sequence, Human Fibroblasts, Clinical Presentation, Clinical Signs, Antiepileptic Drug, Archivos Argentinos De Pediatria, Brain Damage, Age of Onset, Adolescent, Liver diseases, High Frequency, Heart Failure, Pregnancy, Humans, Child, Liver Cirrhosis, Liver, Mutation, Female, Male, Hypoglycemia, Fatty Acid Oxidation, Infant, Follow-up studies, Netherlands, Differential Diagnosis, HELLP Syndrome, Phenotype, Clinical Sciences, Newborn Infant, L-carnitine, Questionnaires, Optometry and Ophthalmology, Public health systems and services research, Survival Rate, Fatty Acid, Health surveys, Multienzyme complexes, Cardiomyopathies, Status Epilepticus, Base Sequence, Human Fibroblasts, Clinical Presentation, Clinical Signs, Antiepileptic Drug, Archivos Argentinos De Pediatria, Brain Damage, Age of Onset