Carnitine Palmitoyltransferase II Deficiency (CPT II) Followed By Rhabdomyolysis and Acute Kidney Injury

BACKGROUND: Carnitine palmitoyltransferase II deficiency (CPT II) is an autosomal recessive disorder and the most common inherited disorder of mitochondrial long-chain fatty acid oxidation, characterised by attacks of myalgia and myoglobinuria. The most common “classic” myopathic form occurs in youn...

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Detalles Bibliográficos
Autores principales: Gjorgjievski, Nikola, Dzekova-Vidimliski, Pavlina, Petronijevic, Zvezdana, Selim, Gjulsen, Dejanov, Petar, Tozija, Liljana, Sikole, Aleksandar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Republic of Macedonia 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5927500/
https://www.ncbi.nlm.nih.gov/pubmed/29731937
http://dx.doi.org/10.3889/oamjms.2018.158

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5927500/
https://www.ncbi.nlm.nih.gov/pubmed/29731937
http://dx.doi.org/10.3889/oamjms.2018.158

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