The revised Ghent nosology for the Marfan syndrome
By B. Loeys, H. Dietz, A. Braverman, B. Callewaert, J. De Backer, R. Devereux, Y. Hilhorst-Hofstee, G. Jondeau, L. Faivre, D. Milewicz and 4 more. Journal of Medical Genetics, 2010
2,035 citations recorded by the source corpus.
Subfields: Cardiology and Cardiovascular Medicine, Genetics, Surgery
View Paper: https://www.semanticscholar.org/paper/23d504c41e7493ee442b2cf48e6bd463ef6bf686
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In Cardiology and Cardiovascular Medicine
Citations in the corpus
- 2020 ESC Guidelines for the management of adult congenital heart disease (2021, methodology): “The diagnosis of Marfan syndrome is based on the Ghent criteria, with aortic root aneurysm/dissection and ectopia lentis as cardinal features.(198) Criteria for the other HTAD entities are less well defined.”