Abstract
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal disease causing hematopoietic cell alteration, caused by a mutation in the PIG-A gene; which does not allow certain important proteins to bind to the cells. A 58-year-old patient presented with headache, a history of malaria, and occasionally dark urine. Magnetic resonance imaging proved to be an effective diagnostic method for detecting renal cortical hemosiderosis, thanks to its high spatial resolution capacity.
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Escariz B., L., Pallasco M., C., Segers, D., Chávez G., V., & Mederos M., K. (2017). Resonancia magnética renal en un paciente con hemoglobinuria paroxística Nocturna. Revista Chilena de Radiologia, 23(2), 55–58. https://doi.org/10.4067/S0717-93082017000200004
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