3-Methylglutaconyl-Coenzyme-A Hydratase Deficiency and the Development of Dilated Cardiomyopathy

A 25-year-old Canadian male with a history of 3-methylglutaconyl-coenzyme-A hydratase deficiency, also known as 3-methylglutaconic aciduria type I, a very rare inborn error of metabolism, presented with respiratory distress, nausea, vomiting and signs of multisystem organ failure due to a suspected...

Descripción completa

Detalles Bibliográficos
Autores principales: Spergel, Craig D., Milko, Mariya, Edwards, Christopher, Steinhoff, Jeff P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358122/
https://www.ncbi.nlm.nih.gov/pubmed/28348715
http://dx.doi.org/10.14740/cr359w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358122/
https://www.ncbi.nlm.nih.gov/pubmed/28348715
http://dx.doi.org/10.14740/cr359w

Ejemplares similares