At least 13 genes mutation has now been identified to cause FHCM. Understanding the molecular genetics mechanisms will provide new avenues for diagnosis and treatment for FHCM.
已发现至少有13种基因的突变可导致家族性肥厚型心肌病，加深对其分子遗传学的认识有利于促进该病的诊断和治疗。
The male patients of FHCM were in multitude (88 89%, 16/18), the family members disease symptoms were severe or light, and the pathologic degrees of the disease were disparity in a family.
家族遗传方面本病以男性患者居多（88.89% ，16 / 18） ，家族成员症状有轻有重、病变程度不一。
Familial hypertrophic cardiomyopathy (FHCM) is a genetically heterogeneous cardiac disease transmitted as an autosomal dominant trait. It is the leading cause of sudden cardiac death (SCD) in youth.
家族性肥厚型心肌病是一种以常染色体显性遗传为特征的具有遗传异质性的心脏疾病，它是年轻人心源性猝死的首要病因。
Familial hypertrophic cardiomyopathy (FHCM) is a genetically heterogeneous cardiac disease transmitted as an autosomal dominant trait. It is the leading cause of sudden cardiac death (SCD) in youth.
家族性肥厚型心肌病是一种以常染色体显性遗传为特征的具有遗传异质性的心脏疾病，它是年轻人心源性猝死的首要病因。
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