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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,...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
The Korean Society of Anesthesiologists
2013
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3790039/ https://ncbi.nlm.nih.gov/pubmed/24101962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4097/kjae.2013.65.3.257 |
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