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Anaesthetic Management of a Patient with Multiple Acetyl CoA Dehydrogenase Deficiency: A Case Report
Multiple acetyl CoA dehydrogenase deficiency is a rare autosomal recessive disorder of amino acid, fatty acid, and choline metabolism. It is a mitochondrial disorder with defective electron transfer flavoproteins or electron transfer flavoprotein dehydrogenases. They are vital for β-oxidation of fat...
Autores principales: | Puthenveetil, Nitu, Joseph, Nandhini, Kottarathil, Vijaykumar Dehannathparambil, Paul, Jerry |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Turkish Society of Anaesthesiology and Reanimation
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361307/ https://www.ncbi.nlm.nih.gov/pubmed/35801333 http://dx.doi.org/10.5152/TJAR.2021.816 |
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