Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) Myopathy Misdiagnosed as Polymyositis
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Rheumatology
Reference5 articles.
1. Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations;J Neurol Neurosurg Psychiatry,2010
2. Lipid storage myopathies;Curr Opin Neurol,2008
3. Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease;Rev Neurol (Paris),2016
4. 162nd ENMC International Workshop: disorders of muscle lipid metabolism in adults 28–30 November 2008, Bussum, the Netherlands;Neuromuscul Disord,2010
5. Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency;Orphanet J Rare Dis,2014
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3. Reasons for misdiagnosis of polymyositis in patients with dysferlinopathy: a clinical case;Neuromuscular Diseases;2022-12-13
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