Rhabdomyolysis caused by carnitine palmitoyltransferase 2 deficiency: A case report and systematic review of the literature
Author:
Affiliation:
1. Critical Care Unit, West Suffolk Hospital, NHS Foundation Trust, Bury St Edmunds, UK
2. Department of Critical Care, Imperial College Healthcare NHS Trust, St Mary's Hospital, London, UK
Abstract
Publisher
SAGE Publications
Subject
Critical Care and Intensive Care Medicine,Critical Care
Link
http://journals.sagepub.com/doi/pdf/10.1177/1751143719889766
Reference44 articles.
1. The Mitochondrial Carnitine Palmitoyltransferase System - From Concept to Molecular Analysis
2. Carnitine palmitoyltransferases 1 and 2: biochemical, molecular and medical aspects
3. Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports
4. Mutations of carnitine palmitoyltransferase II (CPT II) in Japanese patients with CPT II deficiency
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1. Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form;Journal of Pediatric Endocrinology and Metabolism;2023-11-07
2. Myopathic Carnitine Palmitoyltransferase II (CPT II) Deficiency: A Rare Cause of Acute Kidney Injury and Cardiomyopathy;Cureus;2023-10-06
3. Mitochondrial Fatty Acid Beta-Oxidation Disorders in Children: Literature Review;Current Pediatrics;2023-01-20
4. Rhabdomyolysis Associated with Recent SARS-COV-2 Infection in a Patient with Carnitine Palmitoyltransferase II Deficiency;PRILOZI;2022-11-01
5. SEVERE RHABDOMYOLYSIS IN HOMOZYGOTE CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY;EXCLI J;2020
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