Multiple acyl-CoA dehydrogenase deficiency (MADD) presenting as polymyositis
Author:
Affiliation:
1. Rheumatology Department, Royal Adelaide Hospital
2. Discipline of Medicine, University of Adelaide
3. Endocrine and Metabolic Unit, Royal Adelaide Hospital
4. Genetics and Molecular Pathology, Royal Adelaide Hospital, Adelaide, SA, Australia
Publisher
Oxford University Press (OUP)
Subject
Pharmacology (medical),Rheumatology
Link
http://academic.oup.com/rheumatology/article-pdf/59/12/e128/34890138/keaa348.pdf
Reference6 articles.
1. Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency;Cornelius;Hum Mol Genet,2012
2. Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency;Fan;Mol Genet Metab Rep,2018
3. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency;Olsen;Brain,2007
4. Valproic acid metabolism and its effects on mitochondrial fatty acid oxidation: a review;Silva;J Inherit Metab Dis,2008
5. Late onset lipid storage myopathy due to multiple acyl CoA dehydrogenase deficiency triggered by valproate;Papadimitriou;Neuromuscul Disord,1991
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1. Multiple Acyl‐Coenzyme A Dehydrogenase Deficiency Is Associated with Sertraline Use – Is There an Acquired Form?;Annals of Neurology;2024-08-02
2. Late-onset multiple acyl-CoA dehydrogenase deficiency: an insidious presentation;BMJ Case Reports;2023-05
3. Features and diagnostic value of body composition in patients with late-onset multiple acyl-CoA dehydrogenase deficiency;Acta Neurologica Belgica;2022-05-26
4. Sodium-valproate;Reactions Weekly;2021-03
5. Late-onset multiple acyl-CoA dehydrogenase deficiency mimicking myositis in an elderly patient: a case report;BMC Neurology;2020-12
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