年轻健康成年人中伴有左心室心肌致密化不全的BAG-3基因突变型扩张型心肌病
BAG-3 Mutation Dilated Cardiomyopathy With Left Ventricular Noncompaction in Young Healthy Adult.
作者信息
Patel Yash B, David Wadie, Terzic Milan, Mehla Akanksha, Swadia Tanmay V
机构信息
Department of Internal Medicine, Trinity Health Ann Arbor, Michigan, USA.
Department of Cardiology, Ascension Southfield, Michigan, USA.
出版信息
JACC Case Rep. 2024 Nov 20;29(22):102648. doi: 10.1016/j.jaccas.2024.102648.
Cardiomyopathies are generally divided into ischemic and nonischemic types. Dilated cardiomyopathies, which are a type of nonischemic cardiomyopathy, may have a trait of left ventricular noncompaction. We present the case of a 34-year-old man with new-onset decompensated heart failure and left ventricular noncompaction from a BAG3 (Bcl-2 associated athanogene 3) truncating mutation.
心肌病通常分为缺血性和非缺血性类型。扩张型心肌病属于非缺血性心肌病的一种，可能具有左心室心肌致密化不全的特征。我们报告一例34岁男性患者，因BAG3（Bcl-2相关抗凋亡基因3）截短突变导致新发失代偿性心力衰竭及左心室心肌致密化不全。
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