PPA2 deficiency-a rare cause of genetic cardiomyopathy: a case report [0.03%]
PPA2缺乏症-一种罕见的遗传性心肌病病因：病例报告
Sanchaya Khetrapal,Aakash Tuli,Yochitha Pulipati et al.
Sanchaya Khetrapal et al.
Background: PPA2 deficiency is a rare mitochondrial disorder associated with non-ischemic cardiomyopathy, recurrent rhabdomyolysis, and sudden cardiac death (SCD). This case attempts to highlight the diagnostic and manage...
Hisato Takagi
Hisato Takagi
An ST elevation myocardial infarction with multisystemic embolization: a shocking and striking first presentation of antiphospholipid syndrome: a case report [0.03%]
抗磷脂综合征的首次表现竟是急性ST段抬高型心肌梗死合并多系统栓塞：一例个案报告
Meryem Haboub,Ilyas Atlas,Abdenasser Drighil et al.
Meryem Haboub et al.
Introduction: Anti-phospholipid syndrome is characterized by venous and/or arterial thrombosis in the presence of anti-phospholipid antibodies. We report a rare and dramatic manifestation of the syndrome: thrombotic coron...
Kamil Stankowski,Dario Donia,Diego Maceda Penela et al.
Kamil Stankowski et al.
Background: Mitral annular disjunction (MAD), consisting in a systolic separation between the posterior atrial wall-leaflet junction and the basal left ventricular wall, is a disputed imaging entity. MAD was initially ass...
de Winter electrocardiogram pattern evolving into Wellens electrocardiogram pattern in post-percutaneous coronary intervention therapy: a case report [0.03%]
经皮冠状动脉介入治疗后冬冬氏心电图转变为韦尔斯心电图1例报告
Xianghong Ma,Mengwei Bao
Xianghong Ma
Background: The de Winter electrocardiogram (ECG) pattern and Wellens ECG pattern are rare but critical ECG findings, often considered high-risk equivalents of ST-segment elevation myocardial infarction (STEMI) associated...
Arrhythmic mitral annular disjunction or not arrhythmic mitral annular disjunction: that is the problem? [0.03%]
心律失常性主动脉瓣下解剖结构的存在与否？这是一个问题！
Annagrazia Cecere,Martina Perazzolo Marra
Annagrazia Cecere
Supravalvular aortic stenosis mimicking hypertrophic obstructive cardiomyopathy: a case report [0.03%]
主动脉瓣上狭窄误诊为肥厚型心肌病1例报告
Avneesh Sharma,Emily Kaplan,Yaqub Betz et al.
Avneesh Sharma et al.
Background: Hypertrophic cardiomyopathy (HCM) is a relatively common genetic disorder often associated with left ventricular outflow tract (LVOT) obstruction. However, the presence of certain structural abnormalities such...
Pickering syndrome facilitated by seronegative immune mediated necrotizing myopathy: a case report [0.03%]
血清阴性自身免疫相关坏死性肌炎所致的皮克汀氏综合征1例报告
Julija Bienz,Théo Arthur Meister,Rodrigo Soria et al.
Julija Bienz et al.
Background: Immune-mediated necrotizing myopathies (IMNM) are rare types of idiopathic inflammatory myopathies characterized by severe proximal muscle weakness and muscle fibre necrosis with a paucity of inflammatory cell...
Stroke in a 32-year-old male with hypertension, hyperlipoproteinemia(a), and no large vessel disease: a case report [0.03%]
一名高血压和高脂蛋白血症（a型）且无大动脉疾病的32岁男性脑卒中患者病例报告
Zhenwei Gao,Moe Arai,Hanzhang Ma et al.
Zhenwei Gao et al.
Background: Lipoprotein(a) [Lp(a)] is associated with cardiovascular events through three primary mechanisms: promoting atherosclerosis, thrombosis, and inflammation. While evidence of Lp(a)-induced thrombosis in large ve...
Laurna McGovern,Roman Roy,Antonio Rullan
Laurna McGovern