地中海贫血
复合杂合度
医学
血红蛋白
儿科
β地中海贫血
溶血性贫血
突变
遗传学
血红蛋白病
生物
内科学
基因
作者
Catherine Badens,Chantal Paolasso,Chantal Fossat,Henri Wajcman,Isabelle Thuret
出处
期刊:PubMed
[National Institutes of Health]
日期:2005-01-01
卷期号:90 (1): ECR04-ECR04
被引量:6
摘要
We described the case of an infant with compound heterozygozity for a b0-thalassemic mutation and Hemoglobin (Hb) Genova, an unstable Hb variant. He has required regular transfusions as early as the second month of life and since then, behaves like a thalassemia major patient. This association leads to the most severe clinical course involving an unstable variant, reported so far.
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