Medium-chain Acyl-CoA dehydrogenase deficiency presenting with neonatal pulmonary haemorrhage

BACKGROUND: Medium-chain Acyl-CoA dehydrogenase deficiency (MCADD) is the most common inherited disorder of fatty acid beta-oxidation. Signs and symptoms of MCADD typically appear during infancy or early childhood and include vomiting, lethargy, and hypoglycemia. Pulmonary haemorrhage has previously...

Descripción completa

Detalles Bibliográficos
Autores principales: Staels, Willem, D’Haese, James, Sercu, Els, De Meirleir, Linda, Colpaert, Johan, Cornette, Luc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823675/
https://www.ncbi.nlm.nih.gov/pubmed/27057325
http://dx.doi.org/10.1186/s40748-015-0010-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823675/
https://www.ncbi.nlm.nih.gov/pubmed/27057325
http://dx.doi.org/10.1186/s40748-015-0010-9

Ejemplares similares