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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Detalles Bibliográficos
Autores principales: Tandon, Krutika, Tandon, Rahul, Patel, Meet, Parikh, Charmy, Upadhyay, Henil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110299/
https://www.ncbi.nlm.nih.gov/pubmed/33987057
http://dx.doi.org/10.7759/cureus.14407

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110299/
https://www.ncbi.nlm.nih.gov/pubmed/33987057
http://dx.doi.org/10.7759/cureus.14407

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