Abstract
Very long-chain acyl Co-A dehydrogenase deficiency, an inborn error of lipid metabolism, is commonly thought of as a disease of infancy or early childhood. However, several cases of late-onset very long-chain acyl Co-A dehydrogenase have been reported. This report of two military men who survived basic training before their disease presentation broadens the spectrum of late-onset disease, presents two previously unreported mutations, and demonstrates the fine line between athletic, active lifestyle and severe disease presentation. Copyright © by Association of Military Surgeons of U.S., 2006.
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CITATION STYLE
Hoffman, J. D., Steiner, R. D., Paradise, L., Harding, C. O., Ding, L., Strauss, A. W., & Kaplan, P. (2006). Rhabdomyolysis in the military: Recognizing late-onset very long-chain acyl Co-A dehydrogenase deficiency. Military Medicine, 171(7), 657–658. https://doi.org/10.7205/MILMED.171.7.657
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