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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...

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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

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