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...

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Detalles Bibliográficos
Autores principales: Puthenveetil, Nitu, Joseph, Nandhini, Kottarathil, Vijaykumar Dehannathparambil, Paul, Jerry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Society of Anaesthesiology and Reanimation 2022
Materias:
Case ReportPerioperative Care
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

Internet

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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