Multiple Acyl-Coenzyme A Dehydrogenase Deficiency Leading to Severe Metabolic Acidosis in a Young Adult
Author:
Publisher
Elsevier BV
Subject
Endocrinology, Diabetes and Metabolism
Reference18 articles.
1. Multiple acyl-CoA dehydrogenase deficiency;Prasun,2020
2. Inborn Metabolic Diseases: Diagnosis and Treatment;Saudubray,2012
3. Clinical and genetic heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency;Grünert;Orphanet J Rare Dis,2014
4. Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations;Wen;J Neurol Neurosurg Psychiatry,2010
5. A rare presentation of a rare metabolic disorder – multiple acyl CoA dehydrogenase deficiency presenting as rhabdomyolysis and renal failure;Chakraborty;Biomedicine,2021
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