单倍率不足
再生障碍性贫血
免疫学
免疫失调
疾病
医学
免疫系统
细胞毒性T细胞
生物
基因
遗传学
表型
内科学
骨髓
体外
作者
Terje Singsaas Solhaug,Geir E. Tjønnfjord,Kathrine Bjørgo,Odd Kildahl‐Andersen
出处
期刊:Case Reports
[BMJ]
日期:2022-02-01
卷期号:15 (2): e247653-e247653
被引量:3
标识
DOI:10.1136/bcr-2021-247653
摘要
Acquired aplastic anaemia is a rare disease, and occurrence in more than one member of the same family is uncommon. With this case report, we wish to highlight the importance of searching for an underlying genetic cause when this occurs. It may have consequences for future generations in affected families. CTLA4 haploinsufficiency is a heterogeneous disease entity with severe systemic immune dysregulation associated with several autoimmune diseases including aplastic anaemia.
科研通智能强力驱动
Strongly Powered by AbleSci AI