Zobrazeno 1 - 10
of 343
pro vyhledávání: '"Double orifice mitral valve"'
Publikováno v:
JACC: Case Reports, Vol 29, Iss 3, Pp 102204- (2024)
Double-orifice mitral valve (DOMV), a rare congenital heart disease, is the inspiration behind the transcatheter edge-to-edge repair (TEER). Here we report a successful TEER case in a patient with DOMV with severe regurgitation. The patient’s sympt
Externí odkaz:
https://doaj.org/article/35a6e04e26804352aaa81297d8f02929
Publikováno v:
Asian Journal of Surgery, Vol 47, Iss 2, Pp 1119-1120 (2024)
Externí odkaz:
https://doaj.org/article/150cbe9a31fc4760850d106ec6e6a2da
Akademický článek
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Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2023)
Double orifice mitral valve (DOMV) is a rare congenital anomaly that is often associated with cardiac malformation. Valve dysfunction usually presents in childhood; therefore, most cases are diagnosed with DOMV in childhood. Its prevalence and progno
Externí odkaz:
https://doaj.org/article/ea17a1676d2b4d49b6417b161fe6b29c
Publikováno v:
BMC Cardiovascular Disorders, Vol 21, Iss 1, Pp 1-10 (2021)
Abstract Background Patients with both double orifice mitral valve (DOMV) and bicuspid aortic valve (BAV) malformation are rare. Although DOMV or BAV can be detected in some genetic syndromes, it has not been reported to simultaneously appear in Turn
Externí odkaz:
https://doaj.org/article/53299011222344828e6b7d8c113388c8
Publikováno v:
Clinical Case Reports, Vol 10, Iss 5, Pp n/a-n/a (2022)
Abstract Ellis–van Creveld syndrome is a rare autosomal recessive disorder caused by mutations in the EVC and EVC2 genes. The four principal manifestations are chondrodysplasia, polydactyly, ectodermal dysplasia, and congenital heart defects. We de
Externí odkaz:
https://doaj.org/article/60a411da7bd140b49e800319636d3f22
Autor:
Fariba Bayat, Mohammad Hasan Namazi, Mohammad Khani, Shadi Shekarkhar, Aref Fatehi, Mohammadreza Tabary, Isa Khaheshi
Publikováno v:
Clinical Case Reports, Vol 8, Iss 6, Pp 1021-1024 (2020)
Abstract Double orifice mitral valve is a rare condition and may be accompanied by a bicuspid aortic valve (sometimes normal functioning) and coarctation of the aorta. Echocardiography is valuable in detecting the accompanied anomalies. Management de
Externí odkaz:
https://doaj.org/article/0a226f5b14f24b06a4f71053cf6ce5e8
Publikováno v:
Annals of Cardiac Anaesthesia, Vol 24, Iss 4, Pp 487-489 (2021)
Double-orifice mitral valve is a rare congenital anomaly being associated with other cardiac defects and rarely presented in isolation. Valve function can be preserved for long and it is usually an incidental finding. We present an unusual case of do
Externí odkaz:
https://doaj.org/article/d5b70d3ae25846b1a14dd5b90691b04d
Publikováno v:
Annals of Pediatric Cardiology, Vol 13, Iss 2, Pp 174-176 (2020)
Double orifice mitral valve (DOMV) is a rare congenital anomaly of the mitral valve apparatus consisting of an accessory bridge of fibrous tissue, which partially or completely divides the mitral valve into two orifices. It usually occurs as an assoc
Externí odkaz:
https://doaj.org/article/20dce886194945f4bdf9f505eddc16e8
Publikováno v:
Annals of Cardiac Anaesthesia, Vol 22, Iss 2, Pp 215-220 (2019)
Double-orifice mitral valve (DOMV) is an unusual congenital anomaly characterized by a mitral valve with a single fibrous annulus with two orifices or rarely two orifices with two separate mitral annuli opening into the left ventricle. We present a f
Externí odkaz:
https://doaj.org/article/c8652248006a42c189a07b919f68346c