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Journal of Child Neurology
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Combined Partial Deficiencies of Carnitine Palmitoyltransferase II and Mitochondrial Complex I Presenting as Increased Serum Creatine Kinase Level

Chang-Yong Tsao

Department of Pediatrics and Neurology, College of Medicine and Public Health, The Ohio State University, Columbus, Ohio

Jerry R. Mendell

Department of Neurology, College of Medicine and Public Health, The Ohio State University, Columbus, Ohio

Increased serum creatine kinase level is a marker of neuromuscular disorders. When combined with exercise intolerance, muscle cramps, fatigue, myoglobinuria, or muscle weakness, metabolic myopathies of a variety of causes should be considered. We encountered an adolescent male with a persistently high serum creatine kinase level and chronic fatigue who was found to have combined partial defects of carnitine palmitoyltransferase II and mitochondrial complex I. Metabolic myopathy may present with chronic fatigue and a persistently high serum creatine kinase level but without muscle weakness and may be attributable to combined enzyme defects. (J Child Neurol 2002;17:304-306).

Journal of Child Neurology, Vol. 17, No. 4, 304-306 (2002)
DOI: 10.1177/088307380201700414


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