1.
Pediatr Int
; 64(1): e15333, 2022 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36331238
2.
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.).