Achados Radiológicos Hepáticos Associados À Síndrome Osler-Weber-Rendu
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Shovlin CL, Buscarini E, Kjeldsen AD, Mager HJ, Sabba C, Droege F, et al. European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT). Orphanet J Rare Dis. 2018;13:136. doi: 10.1186/s13023-018-0850-2. .
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Schmalz MJ, Radhakrishnan K. Vascular anomalies associated with hepatic shunting. World J Gastroenterol. 2020;26:6582-98. doi: 10.3748/wjg. v26.i42.6582.
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Siddiki H, Doherty MG, Fletcher JG, Stanson AW, Vrtiska TJ, Hough DM, et al. Abdominal findings in hereditary hemorrhagic telangiectasia: pictorial essay on 2D and 3D findings with isotropic multiphase CT. Radiographics. 2008;28:171-84. doi: 10.1148/rg.281075037.
Tortora A, Riccioni ME, Gaetani E, Ojetti V, Holleran G, Gasbarrini A. Rendu- Osler-Weber disease: a gastroenterologist's perspective. Orphanet J Rare Dis. 2019;14:130. doi: 10.1186/s13023-019-1107-4.
McDonald J, Bayrak-Toydemir P, DeMille D, Wooderchak-Donahue W, Whitehead K. Curaçao diagnostic criteria for hereditary hemorrhagic telangiectasia is highly predictive of a pathogenic variant in ENG or ACVRL1 (HHT1 and HHT2). Genet Med. 2020;22:1201-5. doi: 10.1038/s41436-020-0775-8.
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Direitos de Autor (c) 2024 Eulália Antunes, Joana Lopes, Sofia Caridade, Isabel Silva
Este trabalho encontra-se publicado com a Licença Internacional Creative Commons Atribuição 4.0.