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图3.α地中海贫血分类
图3.α地中海贫血分类
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所属报告：
医药生物行业：疾病治疗专题报告二—地中海贫血-250613（26页）.pdf
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图5.东南亚国家和华南地区地中海贫血的流行病学特征
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行业数据
2025-06-16
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图6.地中海贫血市场规模快速增长
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市场规模
2025-06-16
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图20.β-地中海贫血的病理生理及临床表现
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2025-04-25
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2018-1H24华大基因当年地中海贫血基因检测量及同比增
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2025-04-24
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我国南方地区人群地中海贫血基因携带率（%）
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2020-09-27
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地中海贫血筛查的常见方法学对比
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α地中海贫血是由于α珠蛋白链的合成受到部分或完全抑制，导致血红蛋白合成不足而引发的遗传性溶血性贫血，呈常染色体隐性遗传。α地中海贫血的临床表现变异度较大，病情的严重程度与α珠蛋白链减少的程度直接相关，携带者一般表型正常，无症状或仅有轻微的红细胞参数改变，患者可分为中间型α地中海贫血、重型α地中海贫血（Hb Bart′s 胎儿水肿综合征），重型α地中海贫血患者由于功能基因表达时间点的差异，一般在妊娠期或出生后不久死亡。
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医药生物行业：疾病治疗专题报告二—地中海贫血-250613（26页）.pdf
2026年地中海贫血基因治疗行业报告：β地贫市场19亿美元，基因编辑疗法临床进展
表3.慢病毒载体表达β珠蛋白的基因治疗疗法
表2.对BCL11A红系特异性增强子破坏的新兴疗法
表1.针对HBG1/2启动子的新兴疗法开发
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