| Literature DB >> 34304896 |
Hector I Michelena1, Alessandro Della Corte2, Arturo Evangelista3, Joseph J Maleszewski4, William D Edwards4, Mary J Roman5, Richard B Devereux5, Borja Fernández6, Federico M Asch7, Alex J Barker8, Lilia M Sierra-Galan9, Laurent De Kerchove10, Susan M Fernandes11, Paul W M Fedak12, Evaldas Girdauskas13, Victoria Delgado14, Suhny Abbara15, Emmanuel Lansac16, Siddharth K Prakash17, Malenka M Bissell18, Bogdan A Popescu19, Michael D Hope20, Marta Sitges21, Vinod H Thourani22, Phillippe Pibarot23, Krishnaswamy Chandrasekaran24, Patrizio Lancellotti25, Michael A Borger26, John K Forrest27, John Webb28, Dianna M Milewicz17, Raj Makkar29, Martin B Leon30, Stephen P Sanders31, Michael Markl32, Victor A Ferrari33, William C Roberts34, Jae-Kwan Song35, Philipp Blanke36, Charles S White37, Samuel Siu38, Lars G Svensson39, Alan C Braverman40, Joseph Bavaria41, Thoralf M Sundt42, Gebrine El Khoury10, Ruggero De Paulis43, Maurice Enriquez-Sarano24, Jeroen J Bax14, Catherine M Otto44, Hans-Joachim Schäfers45.
Abstract
This International Consensus Classification and Nomenclature for the congenital bicuspid aortic valve condition recognizes 3 types of bicuspid valves: 1. The fused type (right-left cusp fusion, right-non-coronary cusp fusion and left-non-coronary cusp fusion phenotypes); 2. The 2-sinus type (latero-lateral and antero-posterior phenotypes); and 3. The partial-fusion (forme fruste) type. The presence of raphe and the symmetry of the fused type phenotypes are critical aspects to describe. The International Consensus also recognizes 3 types of bicuspid valve-associated aortopathy: 1. The ascending phenotype; 2. The root phenotype; and 3. Extended phenotypes.Entities:
Keywords: aortopathy; bicuspid aortic valve; classification; nomenclature
Mesh：
Year: 2021 PMID： 34304896 DOI： 10.1016/j.jtcvs.2021.06.019
Source DB: PubMed Journal: J Thorac Cardiovasc Surg ISSN： 0022-5223 Impact factor: 6.439