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Carnitine deficiency presenting with encephalopathy and hyperammonemia in a patient receiving chronic enteral tube feeding: a case report

INTRODUCTION: Carnitine is an essential cofactor in mitochondrial fatty acid oxidation. Carnitine deficiency results in accumulation of non-oxidized fatty acyl-coenzyme A molecules, and this inhibits intra-mitochondrial degradation of ammonia. Hyperammonemia may lead to encephalopathy. This scenario...

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Detalles Bibliográficos
Autores principales:	Ling, Peter, Lee, Douglas J, Yoshida, Eric M, Sirrs, Sandra
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432593/ https://www.ncbi.nlm.nih.gov/pubmed/22846666 http://dx.doi.org/10.1186/1752-1947-6-227

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