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A prospective study of mitral valvular prolapse in young men.

作者信息

Sbarbaro J A, Mehlman D J, Wu L, Brooks H L

出版信息

Chest. 1979 May;75(5):555-9. doi: 10.1378/chest.75.5.555.

DOI:10.1378/chest.75.5.555
PMID:436482
Abstract

A cardiac history, a physical examination, an electrocardiogram, phonocardiograms in the supine and standing positions, and an M-mode echocardiogram were obtained in 100 randomly selected, presumably healthy, male medical students (mean age, 26 years). Four percent met standard echocardiographic criteria for mitral valvular prolapse. No midsystolic clicks or late systolic murmurs were appreciated in this group, and none complained of chest pain or palpitations. To elucidate further the clinical implication of the echocardiographic pattern of mitral valvular prolapse, 24-hour ambulatory ECGs, multistage exercise tests, and scintiscans of myocardial perfusion at rest and after exercise (using radioactive 13nitrogen-labelled ammonium) were obtained, with normal results. The absence of life-threatening arrhythmias and exercise-induced abnormalities in these four asymptomatic subjects without abnormal physical findings suggests that the echocardiographic pattern of mitral valvular prolapse in such individuals may represent a variant of normal which does not require extensive evaluation.

摘要

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引用本文的文献

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The prevalence of hypomagnesaemia in pediatric patients with mitral valve prolapse syndrome and the effect of mg therapy.二尖瓣脱垂综合征儿科患者低镁血症的患病率及镁治疗的效果。
Int Cardiovasc Res J. 2012 Sep;6(3):92-5. Epub 2012 Sep 15.
2
Echocardiography in mitral valve disease: a review.二尖瓣疾病的超声心动图检查:综述
Int J Card Imaging. 1985;1(3):189-205. doi: 10.1007/BF01784205.
3
Genetic segregation analysis of familial mitral valve prolapse shows no linkage to fibrillar collagen genes.家族性二尖瓣脱垂的遗传分离分析显示与纤维状胶原基因无连锁关系。
Br Heart J. 1989 Mar;61(3):300-6. doi: 10.1136/hrt.61.3.300.
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Genetic evidence that mutations in the COL1A1, COL1A2, COL3A1, or COL5A2 collagen genes are not responsible for mitral valve prolapse.有基因证据表明,COL1A1、COL1A2、COL3A1或COL5A2胶原蛋白基因的突变与二尖瓣脱垂无关。
Br Heart J. 1989 Mar;61(3):292-9. doi: 10.1136/hrt.61.3.292.