血红蛋白性乙型β地中海贫血综合征

定义 英文原文（暂无中文）

A rare beta-thalassemia associated with another hemoglobin anomaly characterized by the presence of the hemoglobin Lepore variant in association with beta-thalassemia. Clinical presentation is highly variable, depending on the type of beta-thalassemia, and ranges from severe hypochromic microcytic anemia and complete transfusion dependency to moderate, compensated anemia without a need for regular blood transfusions.

别名

Hb乙型-β-地中海贫血综合征

基本事实

遗传方式

常染色体隐性

发病年龄

无数据

外部标识与链接