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Glutaric Aciduria Type II With Ketosis in a Male Infant
Glutaric aciduria type II (GA II) also known as multiple acyl-CoA dehydrogenase deficiency is an inborn metabolic disorder belonging to the family of organic acidurias. It is a disorder that interferes with the body's ability to break down proteins and fats to produce energy. Tandem mass spectr...
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| Vydáno v: | Cureus |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Cureus
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8110299/ https://ncbi.nlm.nih.gov/pubmed/33987057 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.14407 |
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