Literature DB >> 8723060

Familial congenital bicuspid aortic valve: a disorder of uncertain inheritance.

M Clementi1, L Notari, A Borghi, R Tenconi.   

Abstract

Congenital bicuspid aortic valve (BAV) is one of the most frequent heart defects detected by echocardiographic investigation and necropsy (0.9-1% of the general population), but only 16 families with familial congenital BAV have been described up to now. We report on a family in which 4 members of two generations (2 brothers, 1 sister, and her son) are affected with BAV. The BAV mode of inheritance is discussed.

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Year:  1996        PMID: 8723060     DOI: 10.1002/(SICI)1096-8628(19960424)62:4<336::AID-AJMG2>3.0.CO;2-P

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  25 in total

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6.  Endocardial Brg1 disruption illustrates the developmental origins of semilunar valve disease.

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7.  Congenitally bicuspid aortic valve in brothers: coarctation of the aorta with a normally functioning aortic valve in one and no coarctation but severe aortic stenosis in the other.

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8.  Endocarditis with ruptured cerebral aneurysm caused by Cardiobacterium valvarum sp. nov.

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Review 9.  Aortic root disease in athletes: aortic root dilation, anomalous coronary artery, bicuspid aortic valve, and Marfan's syndrome.

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Journal:  Sports Med       Date:  2013-08       Impact factor: 11.136

10.  Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions.

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