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作 者:Andrea Benetti Irene Bertozzi Maria Luigia Randi
机构地区:[1]First Medical Clinic,Department of Medicine – DIMED,University of Padova,Padova 35128,Italy
出 处:《Genes & Diseases》2025年第1期19-21,共3页基因与疾病(英文)
基 金:supported by DOR 2020 funding from the Department of Internal Medicine-DIMED,University of Padua,Padova,Italy.
摘 要:At present,most cases of sporadic absolute erythrocytosis remain without an etiologic demonstration,excluding acquired secondary forms,polycythemia vera,and hereditary erythrocytosis.Therefore,about 70%of all patients with erythrocytosis,receive a diagnosis of idiopathic erythrocytosis(IE)meaning that physicians failed to recognize the cause of the hemoglobin and hematocrit increase.
关 键 词:METABOLISM alterations diagnosis
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