cardiomyopathy是什么意思 cardiomyopathy怎么读
英式：[ˌkɑ:dɪəʊmaɪ'ɒpəθɪ]
美式：[ˌkɑ:dɪəʊmaɪ'ɒpəθɪ]
cardiomyopathy单词基本解析：
n.心肌病n.心肌症
n.心肌病；
cardiomyopathy变化用词：
名词复数: cardiomyopathies |
cardiomyopathy英英释义：
Noun1. a disorder (usually of unknown origin) of the heart muscle (myocardium)
名词 cardiomyopathy:
a disorder (usually of unknown origin) of the heart muscle (myocardium)
同义词：myocardiopathy
cardiomyopathy[ ,kɑ:diəumai'ɔpəθi ]n.a disorder (usually of unknown origin) of the heart muscle (myocardium)
同义词：myocardiopathy
cardiomyopathy中文词源：
cardiomyopathy用法和例句：
Objective To study the surgical treatment of the acromegalic cardiomyopathy.
目的探讨肢端肥大症性心肌病的神经外科手术治疗和疗效.
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Objective To analyze effect of propyl gallate in patients with ischemic cardiomyopathy.
目的研究培丙酯对缺血性心肌病的治疗作用.
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Conclusion Positive surgical treatments can take satisfactory effects on acromegalic cardiomyopathy.
结论肢端肥大症性心肌病经积极的手术治疗能够获得满意的疗效.
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Cardiac fibrosis is the characteristic of the diabetic cardiomyopathy.
心肌纤维化是其重要的病理改变.
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Hypertrophic obstructive cardiomyopathy ( HOCM ) is a kind of disease with unknown etiology.
肥厚性梗阻 型心 肌病是一种原因不明的疾病.
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Objective : To investigate the clinical characteristics and therapy effect of peripartum cardiomyopathy.
目的:分 析总结围产期心肌病的临床特点及其治疗效果.
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Methods: 20 cases of peripartum cardiomyopathy were analyzed retrospectively, and discussed.
方法: 回顾性分析20例围产期心肌病的产科临床和跟踪随访资料.
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Hypertrophic cardiomyopathy occurs when the heart muscle thickens abnormally.
肥厚性心肌病是指心脏肌肉的异常增厚.
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Dilated cardiomyopathy affects the heart's ventricles ( VEN - trih - kuls ) and atria.
扩张性心肌病会影响心房和 心室.
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Objective To observe the effect that growth hormone GH treats dilated cardiomyopathy.
目的观察生长素治疗原发性扩张性心肌病的疗效.
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Arrhythmogenic right ventricular dysplasia ( ARVD ) is a rare type of cardiomyopathy.
致心律失常型右心室发育不良 ( ARVD ) 是一种比较罕见的心肌病.
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Objective Discuss the observation and the nursing method of Dilated cardiomyopathy arrhythmia.
目的讨论扩张型心肌病心律失常的观察及护理方法.
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This article discusses the mechanisms of pathogenesis and therapy of cardiomyopathy.
现就脂毒性心肌病的发病机制及治疗进展做一综述.
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Dilated cardiomyopathy is the most common form of cardiomyopathy.
扩张性心肌病是最为常见的一种心肌病.
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Restrictive cardiomyopathy may result from either myocardial or endomyocardial diseases.
限制性心肌病可以由心肌病变或者心肌内部病变引起.
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cardiomyopathy
Taking Trimetazidine dihydrochloride orally can improve diabetic cardiomyopathy pathogenetic condition, and improve the myocardium tissue constitution and ultramicrostructure.
3. 盐酸曲美他嗪（TD）口服能够改善糖尿病心肌病的病情，使心肌的组织结构及超微结构改善。
Rhabdomyomas of the heart occur in approximately 30% of patients and often present as a congenital cardiomyopathy.
30%的病例具有心脏横纹肌瘤，常表现为先天性的心脏增大。
The absence of left ventricular hypertrophy on echocardiography 30 months earlier makes hypertrophic cardiomyopathy unlikely in a 66-year-old patient.
30个月前患者的心电图没有左室肥大的表现，提示肥厚性心肌病的可能不大。
The volume of left ventricular was decreased (t= 25.4, P< 0.01) with low end -diastolic function in asymmetric hypertrophic cardiomyopathy.
3左室心腔容积较正常降低 ,且舒张能力下降 (t=2 5 .4,P <0 .0 1)。
Verna: Cardiomyopathy?
6但后来我要使被掳的亚扪人归回；
The relationship of the Polymorphism of ALDH2 with alcoholic cardiomyopathy is not confirmed.
ALDH2基因多态性与酒精性心肌病发生的关系未得到证实。
Familial hypertrophic cardiomyopathy (FHC) is an autosomal dominant disease characterized by left ventricular hypertrophy, myofibrillar disarray, and sudden cardiac death.
a心肌肥大症（FHC）是一种体染色体显性遗传的疾病，主要症状为左心室肥大、心肌排列不整，甚至导致猝死。
Cardiomyopathy in DN is associated directly with serum BUN and hypertension.
DN与糖尿病性心肌病的发生时间无并行关系。
Seidman, who is at Harard Medical School, hae identified hundreds of genes with altered expression in preclinical hypertrophic cardiomyopathy.
G.赛德门领头的研究基因修饰小鼠的研究已经确认了在临床前肥厚型心肌病中表达改变的上百个基因。
Tako-tsubo cardiomyopathy was first described in Japan by professor Hikaru Sato. It is characterized by acute chest pain,ST-segment elevation accompanied by reversible apical ballooning in the absence of significant coronary artery disease.
Tako-Tsubo心肌病于1990年由日本的Sato等首次报道,其主要临床表现为胸痛、心电图ST-T改变、可逆性左心室功能障碍和冠脉造影结果正常。
He M,Xu JL,Zheng M,et al.The protective effect of valsartan on cardiomyopathy in type 2 diabetes rats[J].Chin Pharmacol Bull,2004,20(12):1386-9.
[2]何敏,徐济良,郑民,等.缬沙坦对2型糖尿病大鼠心肌病变的防治作用[J].中国药理学通报,2004,20(12):1386-9.
CHEN B,DU FH,LI BQ.The effects of spironolactone on some neurohormonal factors in patients with heart failure secondary to dilated cardiomyopathy[J].Chinese Circulation Journal,2004,19:409-411.
[4]陈斌,杜凤和,李帮清.螺内酯对扩张型心肌病心力衰竭患者某些体液因子的影响[J].中国循环杂志,2004,19:409-411.
"The reason for the cardioprotectie effects of caredilol in anthracycline-induced cardiomyopathy is not fully known," the researchers explain.
“卡维地洛对蒽环类抗生素引起的心肌病病人的心脏保护作用，其作用原理目前还不甚清楚。”
Some people with hypertrophic cardiomyopathy have no symptoms, and the condition does not affect their lives.
一部分的肥厚性心肌病患者没有任何症状，所以这种疾病并不会影响他们的生活。
Correlated study by DCG of two groups shows that seveie ventricle ari-hythmia is increased in the group of primary dilatal cardiomyopathy (DCM).
两组动态心电图(DCG)结果表明,扩张型心肌病(DCM)其心律失常较陈旧性心肌梗塞(OMI)明显。
Clinical symptoms associate cerebellous ataxia, pyramidal syndrome with Babinski sign , abolition of reflexes, disorder of profound sensitivity, dysarthria, oculomotor disorders and cardiomyopathy.
临床症状伴有：小脑共济失调，椎体综合征，如巴宾斯基阳性，反射消失，深度反应失调，构音障碍，眼球运动障碍，以及原发性心肌疾病。
Director：Restrictive cardiomyopathy is characterized by impaired ventricular filling due to increased myocardial stiffness.
主任：限制性心肌病的特点在于心肌硬度增加引起的心室舒张受限。
Resulting mutants were viable at birth but developed dilated cardiomyopathy and died of heart failure within 4 weeks.
产生的突变个体生后可存活，但是会逐渐发展成扩张性心肌病并在4周内死于心衰。
Restrictive cardiomyopathy (RCM) is the least common cardiomyopathy. It is called this because it restricts the heart from stretching and filling with blood properly.
什麽是'限制型心肌病-疾病的预防心脏肌肉完全填补了心'?
EPCs mobilization from bone marrow and augmentation of EPCs in the circulation would have a considerable significance in the treatment of ischemic cardiomyopathy.
从骨髓动员内皮祖细胞,增加循环内皮祖细胞的数量,对治疗缺血性心肌病有重要的临床意义。
He added cardiomyopathy, or the deterioration of the function of the heart muscle, was relatively common in children in the first year of their life.
他补充表示，心肌症(也称做心脏肌肉功能衰竭)，在孩童刚出世的第一年还算常见。
Humor autoimmunity plays a more important role in the pathogenesis of dilated cardiomyopathy by a series of autoantibodies.
其中,体液自身免疫发挥了更重要的作用,一系列的自身抗体参与扩张型心肌病的发病。
Increased morbidity and mortality with acromegaly is associated with cardiovascular complications, hypertension, glucose intolerance, cardiomyopathy and coronary artery disease.
其中包括高血压，葡萄糖耐受性不良，心脏肌肉病变与冠状动脉疾病。
Cirrhosis and pituitary hypogonadism were common in males with this genotype, and one man had cardiomyopathy.
具有这种基因型的男性，肝硬化和脑垂体促性腺功能低下皆很常见，其中一位患有心肌病。
Typical findings include cirrhosis of liver, a bronze-brown pigmentation of the skin, diabetes mellitus, and cardiomyopathy.
典型的症状有肝硬化、皮肤呈青铜色到棕色之色素沉著、糖尿病及心肌病变。
Abstract：Objective To investigate the effects of diltiazem on left ventricular early diastolic flow propagation velocity (VP) in patients with hypertrophic cardiomyopathy (HCM).
刘丽华 王志斌 聂晶 李艳摘要目的 检测硫氮卓酮对肥厚型心肌病（HCM）左心室舒张早期血流传播速度（VP）的影响。
Exertional syncope occurs in aortic stenosis or hypertrophic cardiomyopathy, both of which limit increased cardiac output on exertion.
劳力性晕厥见于主动脉瓣狭窄或肥厚型心肌病，两者都限制活动时心排血量的增加。
Compared last 6 years with first 6 years,the ratios of MI,hypertension and diabetes,RHD,PHD,arrhythmia,cardiomyopathy and CC in the aged patients also have statistic significance.
后6年与前6年相比,老年患者病因中,病因比率明显升高的为心肌梗死、高血压、糖尿病、风心病、肺心病、心肌病,所占比例的差别均有显著性意义(P<0.01)。
The studies of pedigrees have shown dilated cardiomyopathy (DCM) is related with mutation of PLB.
国外两个DCM家系研究发现受磷蛋白基因突变与DCM的发生有关，研究目的旨在探讨中国人群心肌特异性受磷蛋白基因突变与特发性扩张型心肌病发病的关系。
It is the most common genetic cardiac disease,there are at least 11 genes that encode sarcomere proteins,more than 200 types of mutations relate to hypertrophic cardiomyopathy.
在人类,在编码与构成肌小节有关的蛋白质的基因中,现在发现至少有11种基因,超过200种不同的基因突变类型与肥厚型心肌病有关。
Transgene suppression during early postnatal development prevented the development of accessory electrical pathways but not cardiomyopathy or conduction system degeneration.
在出生后发育早期的转基因抑制防止了旁路电通道的发育，但不能防止心肌病或传导系统退化。
In both kinds of hypertrophic cardiomyopathy, the thickened muscle makes the inside of the left ventricle smaller so that it holds less blood.
在所有两种类型的肥厚性心肌病中，左心室心脏肌肉的异常增厚都会导致其内腔的缩小，这样左心室的容血量就会降低。
The use of aldosterone antagonists for dilated cardiomyopathy improves levels of morbidity and mortality.
在扩张型心肌病治疗上加用醛固酮受体拮抗剂可改善发病率和死亡率。
Herein, we report a case of idiopathic left ventricular tachycardia-induced cardiomyopathy treated by catheter ablation and reversed left ventricular function.
在此，我们提出一个因原发性左心室频脉引起之心肌症以电烧灼术成功治疗后，左心室功能恢复正常之案例。
Many cardiac troponin T gene mutations have been found in HCM and DCM, and study of cardiac troponin T gene mutations may help to elucidate the pathogenesis of cardiomyopathy.
在肥厚型和扩张型心肌病中发现了多种心肌肌钙蛋白T的基因突变，围绕心肌肌钙蛋白T的研究有助于阐明心肌病的发病机制。
The important progress of the relationship between genomics and cardiovascular diseases has elucidated several abnormalities of genes leading to familial cardiomyopathy and ion channel diseases.
基因组学与心血管病关系研究的重要进展是阐明导致家族性心肌病和离子通道病的几种基因异常。
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。
In nonobstructive hypertrophic cardiomyopathy, the thickened heart muscle does not block the flow of blood out of the ventricle.
对于非梗阻性的肥厚型心肌病，异常增厚的心脏肌肉并不会阻碍心室将血液输送到全身各处。
For the patients with hypertrophic obstructive cardiomyopathy who are refractory to the standard therapy, permanent pacing as treatment was being paid attention to day by day.
对药物治疗抵抗的肥厚梗阻型心肌病患者,起搏治疗日益受到重视。
The left ventricular diastolic function was determined by ACG in 160 normal persons,50 patients with coronary heart disease,40 with hyperten- sion and 30 with cardiomyopathy.
应用心尖搏动图测定160例正常人及120例冠心病、高血压病和原发性心肌病患者左室舒张功能.
A thorough family history should be taken because many cardiac disorders( eg, coronary artery disease[ CAD], systemic hypertension, bicuspid aortic valve, hypertrophic cardiomyopathy, mitral valve prolapse) have a heritable basis.
很多心脏疾病(冠状动脉疾病(AD)全身性高血压、叶主动脉瓣疾病、厚型心肌病、尖瓣脱垂)有遗传基础，因此应收集详尽的家族病史。
A thorough family history should be taken because many cardiac disorders (eg, coronary artery disease [CAD], systemic hypertension, bicuspid aortic valve, hypertrophic cardiomyopathy, mitral valve prolapse) have a heritable basis.
很多心脏疾病(如冠状动脉疾病(CAD)、全身性高血压、二叶主动脉瓣疾病、肥厚型心肌病、二尖瓣脱垂)都有遗传基础，因此应收集详尽的家族病史。
Echocardiogram is a good way to diagnose hypertrophic cardiomyopathy because it shows the thickened walls of the heart.
心回波图是一个诊断肥厚性心肌病的很不错的方法，因为它能够显示出增厚的心脏肌肉。
Compared with data in control,IVPG in groups of myocardial infarction,dilated cardiomyopathy and coronary heart disease was decreased and CSV left ventricular inflow in these groups was increased significantly(P<(0.001)).
心肌梗死、扩张型心肌病、冠心病各组的IVPG较对照组显著减低,CSV显著增高(P<0.001)。
Mismatches between myocardial fatty acid uptake and utilization lead to the accumulation of cardiotoxic lipid species,and cause lipotoxic cardiomyopathy.
心肌游离脂肪酸的摄入和利用的失协调导致心肌中脂质积聚并进而引起脂毒性心肌病。
Verna: Cardiomyopathy? What does... can you tell me what that is?
心肌炎?能告诉我那是什么吗?
Cardiomyopathy - or another primary disease of the heart muscle.
心肌病:或者其它心肌原发病。
Lipid accumulation in the heart may lead to cardiac dysfunction,which is called lipotoxic cardiomyopathy.
心脏中脂质大量积聚,可以引起心脏功能异常,称之为脂毒性心肌病。
Arrhythmias (23%); hypotension (14%); hypertension, phlebitis (11%); cardiac failure (6%); cardiac arrest, enlarged heart, heart murmur, ischemia, MI, myocarditis, pericarditis, pulmonary hypertension, secondary cardiomyopathy, stroke (3%).
心脏血管：心律不整、低血压、高血压、静脉炎、心脏杂音、心脏扩大、缺氧、心肌梗塞、心包膜炎、中风与心跳停止等。
Taken together, these data provide insight into mechanisms of cardiac PRKAG2 disease and suggest that glycogen-storage cardiomyopathy can be modulated by lowering glycogen content in the heart.
总之，这些数据对于心脏PRKAG2疾病的机制提供了独到的见解，表明可通过降低心脏糖原浓度来调节糖原贮积型心肌病。
We reported a case of LHIS associated with hypertrophic cardiomyopathy, which was suspected a hyperechoic intraa-trial tumor in transthoracic echocardiography.
我们在此提出一个合并脂肪性心房中隔肥大症与肥大性心肌病变的病例，其初始之胸部超音波检查发现为心肌肥大症及高?音之心房肿瘤。
We reported a 71-year-old woman with ampulla cardiomyopathy precipitated by diabeteic ketoacidosis.
我们报告一个由酮酸中毒所引发壶腹型心肌病变于七十一岁女性之个案。
We tested whether serial health status assessments with the Kansas City Cardiomyopathy Questionnaire (KCCQ) can identify patients at increased risk for mortality and hospitalization.
我们拟通过该研究验证是否可以采用堪萨斯州心肌病问卷调查（KCCQ）对患者进行系列健康状况评价，从而对死亡率和入院率风险较高的心衰病人进行识别。
We speculated that mutations in sarcomere protein genes known to cause hypertrophic cardiomyopathy and dilated cardiomyopathy may be associated with left ventricular noncompaction.
我们推测：已知的可导致肥厚性心肌病和扩张性心肌病的肌节蛋白基因突变，可能和左室心肌致密化不全相关。
So we still need to further differentiate the cause of restrictive cardiomyopathy， cardiac fat-pad biopsy and immunoperoxidase staining may be wanted in future treatment .
所以我们需要进一步鉴别限制性心肌的发病原因，日后可能会需要做心脏脂肪垫活检和过氧化酶免疫染色。
Dilated cardiomyopathy (DCM) is characterized by the dilatation of left ventricle or biventrical accompanied by the impairment of the contractile force.
扩张型心肌病(DCM)以左心室或双心室扩张及收缩功能受损为特征,其发病机理主要与病毒感染后的自身免疫反应有关。
Dilated cardiomyopathy(DCM) remains an important problem,which is complex,multifactoral process consisting of viral continuous infection and autoimmunity.
扩张型心肌病一直是心血管领域的难点,其发病机制包括病毒的持续感染致心肌炎转化和自身免疫等。
Prolonged overactivation of neurohormonal mechanisms in dilated cardiomyopathy is harmful to the cardiovascular system and leads to poor prognosis.
扩张型心肌病患者神经激素长期过度激活机制对心血管系统产生不良作用,导致预后不佳。
Dilated cardiomyopathy is a disease of heart muscle resulting in atrial and ventricular dilation.
扩张型心肌病是指心肌异常引起的心房和心室扩张。
Dilated cardiomyopathy affects the heart's ventricles (VEN-trih-kuls) and atria.
扩张性心肌病会影响心房和心室。
To assess the cardiac functional changes in patients with dilated cardiomyopathy measured by a newly developed Doppler tissue imaging (DTI) and to compare the sensitivity and reliability of DTI with conventional function al indices.
探讨扩张型心肌病（DCM）的心功能变化，比较多普勒组织显像（DTI）与传统心功能指标的敏感性及可靠性。
To evaluate effects of selective Bisoprolol on baroreceptor in patients withheart failure secondary to dilated cardiomyopathy (DCM).
探讨比索洛尔治疗心力衰竭时对对压力感受器功能的影响。
To observe the effect of carvedilol on transmural heterogeneity of ventricular repolarization in dilated cardiomyopathy (DCM), 24 rabbits were randomly divided into DCM, carvedilol and control groups.
摘要为观察卡维地洛对扩张型心肌病跨室壁复极不均一性的作用，将24只家兔随机分为扩张型心肌病组、卡维地洛组和正常对照组。
Sustained chronic tachyarrhythmias often lead to cardiac dysfunction known as tachycardia-induced cardiomyopathy or tachycardiomyopathy.
摘要持续性的心搏过速会造成心脏功能变差，称之为心搏过速引发之心肌症。
Objective To improve diagnostic level of rare cases during antiretroviral therapy, we analyze the clinical and laboratory characters of dilated cardiomyopathy caused by AZT.
摘要目的为了提高艾滋病抗病毒治疗过程中罕见病例的诊断水平，本文分析了齐多夫定(AZT)所致心肌病的临床和实验室检查特点。
Objective To report the electroanatomic characteristics and outcome of ablative therapy in 2 patients with arrhythmogenic right ventricular cardiomyopathy (ARVC).
摘要目的报道2例致心律失常右室发育不良心肌病(ARVC)的电生理特征及导管消融结果。
Objective To explore the roles of heat shock protein 60(HSP60) in myocardial tissue and serum anti-human HSP60 antibody in the initiation and progression of dilated cardiomyopathy (DCM).
摘要目的探讨扩张型心肌病(DCM)心肌组织中HSP60以及血清中抗人HSP60抗体在DCM发生、发展中的作用。
Objective To explore etiology and pathogenesis of viral myocarditis (VMC) and dilated cardiomyopathy (DCM).
摘要目的探讨病毒性心肌炎(VMC)和扩张性心肌病(DCM)的发病机制及相互关系。
Objective: To explore some indices for geometric evaluating left ventricular remodeling and their relationship with left ventricular function in dilated cardiomyopathy (DCM).
摘要目的：探讨扩张型心肌病（DCM）左心室几何重构的形态学评价指标及其与心功能的关系。
Methods:1.5 Tesla MR (Siemems Company) with ARGUS software was used on 17 cases with elder coronary heart disease (CHD) 5 cases, hypertrophic cardiomyopathy (HCM) and 8 volunteers.
方法 :使用德国Siemems公司 1.5TeslaMR扫描仪 ,ARGUS软件对 17例老年冠心病患者 ,5例肥厚型心肌病患者 ,8例健康志愿者进行研究。
Methods Retrospective analysis on 41 cases of PTSMA for hypertrophic obstructive cardiomyopathy (HOCM) was performed.
方法 回顾性分析41例肥厚性梗阻型心肌病（HOCM）患者行PTSMA的临床资料。
Methods Totally 42 patients with LVH,including 16 with hypertrophic cardiomyopathy(HCM) and 26 with hypertensive heart disease(HHD)were studied,and 20 normal volunteers were as the control(NC).
方法 左室肥厚患者4 2例,包括肥厚型心肌病( HCM) 1 6例和高血压性心脏病( HHD)左室肥厚2 6例; 正常对照( NC) 2 0例。
Me- thods 42 patients with hypertrophic cardiomyopathy and 36 age matched normal subjects underwent TVI studied.
方法 应用QTVI获取 36例正常人和 4 2例HCM患者左室长轴方向不同室壁心肌多普勒速度曲线。
Methods: 20 cases of peripartum cardiomyopathy were analized retrospectively,and discussed.
方法:回顾性分析20例围产期心肌病的产科临床和跟踪随访资料。
Methods From 1998 to 2002,28 cases of hypertrophic cardiomyopathy were studied by comparison of Doppler echocardiography, CT, MR1 and clinical findings.
方法对比分析1998年-2002年诊治的28例肥厚型心肌病患者的多普勒超声心动图、CT或核磁共振检查资料、动态心电图和临床表现。
Methods:Myocardial ultrasonic backscatter parameters of 37 hypertension(HT)patients,15 hypertrophic cardiomyopathy (HCM) patients with hypertrophic interventricular septum and 40 normal were measured.
方法：本研究测定了37例高血压病患者、15例肥厚部位为室间隔的肥厚型心肌病患者及40例正常对照者的心肌超声背向散射参数。
Methods: A total of 30 patients with hypertrophic cardiomyopathy were assigned to Kelangning group (20 cases) or routine treatment group (10 cases).
方法：肥厚型心肌病30例，分为：治疗组（20例，用克朗宁治疗）和常规治疗组（10例，常规方法治疗），比较两组疗效。
It was often misdiagnosed as coronary artery disease, rheumatic heart disease, hypertensive heart disease and expansive cardiomyopathy.
易误诊为冠心病、风心病、高心病和扩张型心肌病等。
A 16-year-old girl with cardiomyopathy asks Fish to petition a judge to allow her father, who's in prison for murdering her mother, to donate his heart to save her.
有一个十六岁有心肌症的女孩来找李察，希望他可以替她申请准许她父亲损出器官给她，她的父亲是一个谋杀犯，并身上监狱。
One Group A athlete died suddenly of arrhythmogenic right ventricular cardiomyopathy while participating in a field hockey game against medical advice.
有一位A组的运动员由于不听从医生的建议，在参加一场野外曲棍球赛时，因心律不整的右心室心肌病而猝死。
用作名词(n.)CVB infection may be one of the causes of peripartum cardiomyopathy.
CVB感染可能是围生期心肌病的病因之一。