Zobrazeno 1 - 10
of 151
pro vyhledávání: '"subaortic membrane"'
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background Double chambered right ventricle is a rare congenital heart disease that is characterised by the presence of an anomalous muscle bundle that divides the right ventricle into a low pressure superior (distal) chamber and a high pres
Externí odkaz:
https://doaj.org/article/7e8fa11d5f58400386c755f95fbabd94
Akademický článek
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Publikováno v:
Heart Views, Vol 23, Iss 1, Pp 60-66 (2022)
A 35-year-old pregnant female in her second trimester presented with heart failure manifestations with evidence of very severe fixed left ventricular outflow tract obstruction. The peak systolic gradient was 132 mmHg, which is the highest reported in
Externí odkaz:
https://doaj.org/article/c362fc41bc4e4563838ce46004230a7f
Autor:
Johanna Schlein, Felix Wollmann, Alexandra Kaider, Dominik Wiedemann, Harald Gabriel, Stephan Hornykewycz, Eva Base, Ina Michel-Behnke, Günther Laufer, Daniel Zimpfer
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
ObjectivesSubvalvular aortic stenosis (SAS) can occur as discrete or tunnel-like obstruction of the left ventricular outflow tract and as progressive disease often leads to aortic valve regurgitation. We report our 30-year single-center experience af
Externí odkaz:
https://doaj.org/article/acfc210856e645baa2d2d3912a4d64a8
Akademický článek
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Complex and multilevel left ventricular outflow tract obstruction: What can 3D echocardiography add?
Autor:
Hoda Abdelgawad, Mahmoud Shehata, Mahmoud Abdelnabi, Abdallah Almaghraby, Mohamed Ayman Abdel-Hay
Publikováno v:
The Egyptian Heart Journal, Vol 73, Iss 1, Pp 1-11 (2021)
Abstract Background Subaortic obstruction by a membrane or systolic anterior motion of the mitral valve leaflets is usually suspected in young patients, especially if the anatomy of the aortic valve is not clearly stenotic and unexplained left ventri
Externí odkaz:
https://doaj.org/article/2516c00ed48c46d9b27b79952f37b934
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
Autor:
Lulu Abushaban, Babu Uthaman, John Puthur Selvan, Mustafa Al Qbandi, Prem N Sharma, Thinakar Vel Mariappa
Publikováno v:
Annals of Pediatric Cardiology, Vol 12, Iss 3, Pp 212-219 (2019)
Background: Studies of long-term outcomes of discrete subaortic stenosis (DSS) are rare. Therefore, we reviewed the long-term outcomes of subaortic membrane resection in children with isolated DSS over 16 years from a single institution. Materials an
Externí odkaz:
https://doaj.org/article/1f7fb5ffe331419aa831684d58b027f2
Autor:
Agnes S. Kim, Katharine J. Henderson, Sumeet Pawar, Min Jung Kim, Shahnaz Punjani, Jeffrey S. Pollak, John T. Fahey, Guadalupe Garcia‐Tsao, Lissa Sugeng, Lawrence H. Young
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 9, Iss 20 (2020)
Background Patients with hereditary hemorrhagic telangiectasia have liver vascular malformations that can cause high‐output cardiac failure (HOCF). Known sequelae include pulmonary hypertension, tricuspid regurgitation, and atrial fibrillation. Met
Externí odkaz:
https://doaj.org/article/9e117051f89748ec8e33003bb18d3982
Autor:
Aviva Levitas, Liam Aspit, Neta Lowenthal, David Shaki, Hanna Krymko, Leonel Slanovic, Ronit Yagev, Ruti Parvari
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 10; Pages: 8864
Weill–Marchesani syndrome (WMS) is a rare genetic inherited disorder with autosomal recessive and dominant modes of inheritance. WMS is characterized by the association of short stature, brachydactyly, joint stiffness, eye anomalies, including micr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::add370439ee3c456ab00ed58e9dd7c79