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

• Asıl Yazarlar: Jingyi QIAO (Yazar), Jian MING (Yazar), Jiaqi YUAN (Yazar), Bingxing LUO (Yazar), Junling WENG (Yazar), Juntao YAN (Yazar), Yingyao CHEN (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Editorial Office of Chinese Journal of Public Health, 2023-10-01T00:00:00Z.
• Konular: article
• Online Erişim: 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...