Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia

Autor: Justin P. McWilliams, Miles Conrad, Mary Porteous, Mary E. Meek, James R. Gossage, Jay F. Piccirillo, Masaki Komiyama, Elisabetta Buscarini, Carlo Sabbà, Andrea Lausman, Paul J. Rochon, Ketil Heimdal, Rose Pantalone, Claire L. Shovlin, Valerie A. Palda, Hanny Al-Samkari, Kevin Korenblatt, Marianne S. Clancy, Jamie McDonald, Katharine J. Henderson, Marie E. Faughnan, Claudia Crocione, Steven W. Hetts, Erik Deslandres, Urban W. Geisthoff, Ingrid Winship, Els de Gussem, Vivek N. Iyer, Daniel Cortes, Sophie Dupuis-Girod, Beth Plahn, Kelly Lang-Robertson, Patrick Foy, Mark S. Chesnutt, Ivan Radovanovic, Anette Drøhse Kjeldsen, Felix Ratjen, Johannes J. Mager, Carol Derksen, Adrienne M. Hammill, Sara Palmer, Marcelo M. Serra, Jack McMahon, Josanna Rodriguez-Lopez, Andrew J. White, Roberto Zarrabeitia, Raj S. Kasthuri, Marco C. Post, Jama M. Darling, Scott E. Olitsky, Dennis L. Sprecher, Murali M. Chakinala, Kevin J. Whitehead, David M. Poetker, Meir Mei-Zahav

Publikováno v: Faughnan, M E, Mager, J J, Hetts, S W, Palda, V A, Lang-Robertson, K, Buscarini, E, Deslandres, E, Kasthuri, R S, Lausman, A, Poetker, D, Ratjen, F, Chesnutt, M S, Clancy, M, Whitehead, K J, Al-Samkari, H, Chakinala, M, Conrad, M, Cortes, D, Crocione, C, Darling, J, de Gussem, E, Derksen, C, Dupuis-Girod, S, Foy, P, Geisthoff, U, Gossage, J R, Hammill, A, Heimdal, K, Henderson, K, Iyer, V N, Kjeldsen, A D, Komiyama, M, Korenblatt, K, McDonald, J, McMahon, J, McWilliams, J, Meek, M E, Mei-Zahav, M, Olitsky, S, Palmer, S, Pantalone, R, Piccirillo, J F, Plahn, B, Porteous, M E M, Post, M C, Radovanovic, I, Rochon, P J, Rodriguez-Lopez, J, Sabba, C, Serra, M, Shovlin, C, Sprecher, D, White, A J, Winship, I & Zarrabeitia, R 2020, ' Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia ', Annals of Internal Medicine, vol. 173, no. 12, pp. 989-1001 . https://doi.org/10.7326/M20-1443

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease with an estimated prevalence of 1 in 5000 that is characterized by the presence of vascular malformations (VMs). These result in chronic bleeding, acute hemorrhage, and comp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4ee4994475518c545cc94de43b382bf
https://doi.org/10.7326/m20-1443