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Year: 2018

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Type: Article

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

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Author: Gjorgjievski, Nikola
Author: Dzekova Vidimliski, Pavlina
Author: Petronijevic, Zvezdana
Author: Selim, Gjulshen
Author: Dejanov, Petar
Author: Tozija, Liljana
Author: Shikole, Aleksandar

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Abstract: 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 young adults and is characterised by recurrent episodes of rhabdomyolysis triggered by prolonged exercise, fasting or febrile illness.

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Publisher: Scientific Foundation SPIROSKI

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Relation: Open Access Macedonian Journal of Medical Sciences

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Identifier: oai:repository.ukim.mk:20.500.12188/14600
Identifier: 1857-9655
Identifier: http://hdl.handle.net/20.500.12188/14600
Identifier: 10.3889/oamjms.2018.158
Identifier: https://spiroski.migration.publicknowledgeproject.org/index.php/mjms/article/download/oamjms.2018.158/2044
Identifier: https://spiroski.migration.publicknowledgeproject.org/index.php/mjms/article/download/oamjms.2018.158/2017
Identifier: 6
Identifier: 4
Identifier: 666
Identifier: 668

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