摘要
目的分析一个家族性心房纤颤家系的遗传学特点。方法查此家族成员的病史,记录心电图,绘制家系图。结果该家系3代19人中有6人患有心房纤颤。结论经过遗传分析,认为该家系属于常染色体显性遗传。
Objective To investigate the genetic characters of a pedigree′s familial atrial fibrillation. Methods The family members were investigated about the formal medical history and ECGs were recorded in order to draw the pedigree diagram. Results 6 out of 19 among three generations suffered from atrial fibrillation. Conclusion Genetic analysis concluded that this disease was caused by autosomal dominant inheritance.
出处
《中国全科医学》
CAS
CSCD
北大核心
2012年第2期182-183,共2页
Chinese General Practice
关键词
心房颤动
系谱
常染色体显性遗传
Atrial fibrillation
Pedigree
Autosomal dominant inheritance
