Hereditary hemorrhagic telangiectasia (Osler’s disease): systemic, interdisciplinary, relatively common—and often missed

Author:

Geisthoff Urban W.,Mahnken Andreas H.,Denzer Ulrike W.,Kemmling André,Nimsky Christopher,Stuck Boris A.

Publisher

Deutscher Arzte-Verlag GmbH

Reference73 articles.

1. Droege F, Kuerten CHL, Kaiser C, et al.: Hereditäre hämorrhagische Teleangiektasie: Symptome und diagnostische Latenz. Laryngorhinootologie 2021; 100: 443–52.

2. de Gussem EM, Kroon S, Hosman AE, et al.: Hereditary hemorrhagic telangiectasia (HHT) and survival: the importance of systematic screening and treatment in HHT centers of excellence. J Clin Med 2020; 9: 3581.

3. de Gussem EM, Edwards CP, Hosman AE, et al.: Life expextancy of parents with hereditary haemorrhagic telangiectasia. Orphanet J Rare Dis 2016; 11: 46.

4. Faughnan ME, Mager JJ, Hetts SW, et al.: Second international guidelines for the diagnosis and management of hereditary hemorrhagic telangiectasia. Ann Intern Med 2020; 173: 989–1001.

5. Faughnan ME, Palda VA, Garcia-Tsao G, et al.: International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet 2011; 48: 73–87.

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