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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Hlavní autoři: Oliveira, Sara Freitas, Pinho, Liliana, Rocha, Hugo, Nogueira, Célia, Vilarinho, Laura, Dinis, Maria José, Silva, Conceição
Médium: Artigo
Jazyk:Inglês
Vydáno: PAGEPress Publications, Pavia, Italy 2013
Témata:
Case Report
On-line přístup: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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