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JACC Case Rep ; 3(17): 1863-1868, 2021 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-34917969

RESUMO

A man affected by hereditary hemorrhagic telangiectasia who had chronic severe hypoxemia is presented. This hypoxemia was synergistically caused by high-output heart failure due to severe hepatic shunts and multiple pulmonary arteriovenous shunts. The symptomatic combination is rare, and genetic testing showed a novel endoglin mutation. (Level of Difficulty: Advanced.).

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