结合性遗传球细胞和β-thalassaemia特征:一种罕见的共存特征
Iffat Jamal1, Shuchismita1, Vijayanand Choudhary1
1Department of Haematology Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India.
The National medical journal of India
|June 30, 2025
概括
贝塔血症特征 (BTT) 是印度血液溶解性贫血的常见原因,通常没有被诊断出来. 早期检测BTT和同时发生的遗传球细胞分裂对于遗传咨询和减少出生缺陷至关重要.
科学领域:
- 血液学 血液学 血液学
- 医学遗传学 医学遗传学
背景情况:
- 血球蛋白病是印度最常见的溶血性疾病,其中β-thalassaemia特征 (BTT) 是最常见的遗传性溶血性贫血.
- 遗传传染病常常呈现无症状,导致诊断延迟和遗传咨询机会错过.
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