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...

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Detalles Bibliográficos
Autores principales: Rajakumar, Akila, Kaliamoorthy, Ilankumaran, Reddy, Mettu Srinivas, Rela, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Case Report
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

Internet

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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