Journal of pediatric hematology/oncologyHumansHemochromatosisbeta-ThalassemiaRetrospective StudiesMale
Increased Red Blood Cell Count With High Hemoglobin Indicates a Different Diagnosis From Beta-thalassemia Trait, Regardless of Mean Corpuscular Volume: Hereditary Hemochromatosis-A Retrospective Analysis.
Deniz Aslan, Ali Kadir Koç, Ferda Emriye Perçin
Published: 202610.1097/MPH.0000000000003138
Abstract
Hereditary hemochromatosis (HH) is an iron storage disorder characterized by increased iron absorption leading to elevated erythrocyte parameters, including red blood cell (RBC) count. It is the most common genetic disorder in Caucasians and is preva…
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