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,...
Salvato in:
| Autori principali: | , , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Korean Society of Anesthesiologists
2013-09-01
|
| Serie: | Korean Journal of Anesthesiology |
| Soggetti: | |
| Accesso online: | http://ekja.org/upload/pdf/kjae-65-257.pdf |
| Tags: |
Nessun Tag, puoi essere il primo ad aggiungerne!!
|