• Am. J. Med. Sci. · Jul 2020

    Review Case Reports

    Severe Rhabdomyolysis in Glucose-6-Phosphate Dehydrogenase Deficiency.

    • Balraj Singh, Parminder Kaur, Kok Hoe Chan, Robert G Lahita, Michael Maroules, and Chandra Chandran.
    • Department of Hematology/Oncology, Saint Joseph University Medical Center, Paterson, New Jersey.
    • Am. J. Med. Sci. 2020 Jul 1; 360 (1): 72-74.

    AbstractGlucose-6-Phosphate Dehydrogenase (G6PD) deficiency is an X-linked genetic disorder associated with intravascular hemolysis. Rhabdomyolysis with myoglobinuria in a patient with G6PD deficiency is a very rare manifestation, in fact, to the best of our knowledge, only a few case reports have been published in the literature to date. Herein, we report an unusual presentation of a 33-year-old male with G6PD deficiency with multiple episodes of severe rhabdomyolysis with no significant concurrent hemolysis. This case supports the hypothesis that rhabdomyolysis may be a rare manifestation of G6PD deficiency, though the exact causation still remains unclear.Copyright © 2020 Southern Society for Clinical Investigation. Published by Elsevier Inc. All rights reserved.

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