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    Second international guidelines for the diagnosis and management of hereditary hemorrhagic telangiectasia

    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.
    Ann. intern. med; 173 (12), 2020
    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 complications from shunting through VMs. The goal of the Se...
    Télangiectasie hémorragique héréditaire/prévention et contrôle, Télangiectasie hémorragique héréditaire/génétique, Anomalies vasculaires/génétique, Épistaxis/prévention et contrôle, Muqueuse nasale, Hémorragie gastro-intestinale/prévention et contrôle
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