Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a severe fatty acid oxidation disorder

Keyphrases

• Medium-chain acyl-CoA Dehydrogenase Deficiency 100%
• Fatty Acid Oxidation Disorders 100%
• Clinical Symptoms 50%
• Asymptomatic Hypoglycemia 50%
• Differential Diagnosis 50%
• Aciduria 50%
• Acyl-CoA Dehydrogenase 50%
• Dehydrogenase Deficiency 50%
• Skin Fibroblasts 50%
• Cultured Skin 50%
• Therapeutic Regimen 50%
• Long-chain Acylcarnitines 50%
• Fatal Outcome 50%
• Carnitine Deficiency 50%
• Hepatopathy 50%

Pharmacology, Toxicology and Pharmaceutical Science

• Fatty Acid 100%
• Long Chain 3 Hydroxyacyl Coenzyme A Dehydrogenase 100%
• Acylcarnitine 50%
• Hypoglycemia 50%
• Fatality 50%
• Aciduria 50%
• 3 Hydroxyacyl Coenzyme A Dehydrogenase 50%
• Carnitine Deficiency 50%

Biochemistry, Genetics and Molecular Biology

• Beta Oxidation 100%
• 3-Hydroxyacyl-CoA Dehydrogenase 100%
• Blood Plasma 50%
• Fibroblast 50%