Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation–Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase Deficiency

Encephalopathy and Myopathy in children of varying ages can be due to variety of causes including Mitochondrial diseases, metabolic diseases like renal tubular acidosis, storage diseases as well as fatty acid oxidation (FAO) disorders. FAO related disorders have variable clinical presentation and ma...

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Detalles Bibliográficos
Autores principales: Chandra, Sadanandavalli R., Christopher, Rita, Narayanappa, Gayathri, Ramanujam, Nitin C., Katragadda, Pavan, Huddar, Akshata, Jha, Shreyashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144612/
https://www.ncbi.nlm.nih.gov/pubmed/30271477
http://dx.doi.org/10.4103/JPN.JPN_21_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144612/
https://www.ncbi.nlm.nih.gov/pubmed/30271477
http://dx.doi.org/10.4103/JPN.JPN_21_18

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