Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency

Very long chain acyl CoA dehydrogenase deficiency (VLCADD) is an inborn error in long chain fatty acid oxidation with significant variability in the severity and timing of its clinical presentation. Neonatal presentations of VLCADD have included hypoglycemia and cardiomyopathy while rhabdomyolysis i...

Descripción completa

Detalles Bibliográficos
Autores principales: Scott Schwoerer, Jessica, Cooper, Gena, van Calcar, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750558/
https://www.ncbi.nlm.nih.gov/pubmed/26937394
http://dx.doi.org/10.1016/j.ymgmr.2015.03.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750558/
https://www.ncbi.nlm.nih.gov/pubmed/26937394
http://dx.doi.org/10.1016/j.ymgmr.2015.03.003

Ejemplares similares