Late-onset multiple acyl-CoA dehydrogenase deficiency with cardiac syncope: A case report
Author:
Publisher
Baishideng Publishing Group Inc.
Subject
General Medicine
Reference23 articles.
1. Heterogeneous Phenotypes in Lipid Storage Myopathy Due to ETFDH Gene Mutations
2. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency
3. An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency
4. Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency
5. Clear relationship betweenETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency
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2. Cardiogenic shock and asphyxial cardiac arrest due to glutaric aciduria type II;World Journal of Emergency Medicine;2023
3. Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic Review;Frontiers in Pediatrics;2021-05-10
4. ETF dehydrogenase advances in molecular genetics and impact on treatment;Critical Reviews in Biochemistry and Molecular Biology;2021-04-07
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