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Anaesthetic considerations for liver transplantation in propionic acidemia
Propionic acidemia (PA) is an autosomal recessive disorder of metabolism due to deficiency of the enzyme propionyl-CoA carboxylase (PCC) that converts propionyl-CoA to methylmalonyl-CoA with the help of the cofactor biotin inside the mitochondria. The resultant accumulation of propionyl-CoA causes s...
Autores principales: | Rajakumar, Akila, Kaliamoorthy, Ilankumaran, Reddy, Mettu Srinivas, Rela, Mohamed |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782424/ https://www.ncbi.nlm.nih.gov/pubmed/26962256 http://dx.doi.org/10.4103/0019-5049.174799 |
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