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Rhabdomyolysis as a Presenting Manifestation of Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Very long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency (MIM 201475) is a rare inherited disorder with three forms of clinical presentation: a severe early-onset form; an intermediate form with childhood onset; and an adult-onset form, of mild severity. During adolescence and adulthood, exe...

詳細記述

保存先:
書誌詳細
主要な著者: Oliveira, Sara Freitas, Pinho, Liliana, Rocha, Hugo, Nogueira, Célia, Vilarinho, Laura, Dinis, Maria José, Silva, Conceição
フォーマット: Artigo
言語:Inglês
出版事項: PAGEPress Publications, Pavia, Italy 2013
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3981269/
https://ncbi.nlm.nih.gov/pubmed/24765510
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/cp.2013.e22
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