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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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Pubblicato in:Cureus
Autori principali: Tandon, Krutika, Tandon, Rahul, Patel, Meet, Parikh, Charmy, Upadhyay, Henil
Natura: Artigo
Lingua:Inglês
Pubblicazione: Cureus 2021
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Accesso online: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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