Intractable metabolic acidosis in a child with propionic acidemia undergoing liver transplantation -a case report-

Propionic acidemia (PA) is a rare autosomal recessive disorder of metabolism caused by deficient activity of the mitochondrial enzyme propionyl-CoA carboxylase. The clinical manifestations are metabolic acidosis, poor feeding, lethargy, vomiting, osteoporosis, neurological dysfunction, pancytopenia,...

Descripción completa

Detalles Bibliográficos
Autores principales: Ryu, Jiyoung, Shin, Young Hee, Ko, Justin Sangwook, Gwak, Mi Sook, Kim, Gaab-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Anesthesiologists 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790039/
https://www.ncbi.nlm.nih.gov/pubmed/24101962
http://dx.doi.org/10.4097/kjae.2013.65.3.257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790039/
https://www.ncbi.nlm.nih.gov/pubmed/24101962
http://dx.doi.org/10.4097/kjae.2013.65.3.257

Ejemplares similares