Progress in researches on disease burden and health service utilization of beta-thalassemia patients in China

• Κύριοι συγγραφείς: Jingyi QIAO (Συγγραφέας), Jian MING (Συγγραφέας), Jiaqi YUAN (Συγγραφέας), Bingxing LUO (Συγγραφέας), Junling WENG (Συγγραφέας), Juntao YAN (Συγγραφέας), Yingyao CHEN (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: Editorial Office of Chinese Journal of Public Health, 2023-10-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: Connect to this object online.

Thalassemia is an inherited hemoglobin disorder clinically categorized into alpha and beta thalassemia. Severe beta-thalassemia patients commonly experience anemia during infancy and progressively deteriorate, necessitating long-term blood transfusion to sustain life. The reliance on the blood trans...