Pulmonary Hypertension and Hereditary Hemorrhagic Telangiectasia Related to an ACVRL1 Mutation

Pulmonary hypertension and hereditary hemorrhagic telangiectasia (HHT) have an association mediated by activin A receptor type II-like 1 (ACVRL1) gene pathogenic variants. A 30-year-old woman was previously admitted to a hospital due to lung hemorrhage, and was diagnosed with pulmonary hypertension,...

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Detalles Bibliográficos
Autores principales: Yokokawa, Tetsuro, Sugimoto, Koichi, Kimishima, Yusuke, Misaka, Tomofumi, Yoshihisa, Akiomi, Morisaki, Hiroko, Yamada, Osamu, Nakazato, Kazuhiko, Ishida, Takafumi, Takeishi, Yasuchika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7008044/
https://www.ncbi.nlm.nih.gov/pubmed/31511490
http://dx.doi.org/10.2169/internalmedicine.3625-19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7008044/
https://www.ncbi.nlm.nih.gov/pubmed/31511490
http://dx.doi.org/10.2169/internalmedicine.3625-19

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