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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...
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| 主要な著者: | , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
PAGEPress Publications, Pavia, Italy
2013
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| 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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