Life-threatening hemoptysis: case of Osler–Weber–Rendu Syndrome

Hereditary haemorrhagic telangiectasia (HHT), also known as Osler–Weber–Rendu syndrome, is a rare autosomal dominant vascular disorder. Patients with HHT may present with a wide spectrum of clinical manifestations, some considered to be life-threatening. We present the case of a 53-year-old male who...

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Bibliografiset tiedot
Julkaisussa:Oxf Med Case Reports
Päätekijät: Alicea-Guevara, Ricardo, Cruz Caliz, Michael, Adorno, Jose, Fernandez, Ricardo, Rivera, Kelvin, Gonzalez, Gustavo, Hernandez-Castillo, Ricardo Alan, Fernandez, Rosangela, Castillo Latorre, Christian
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2018
Aiheet:
Case Report
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5865522/
https://ncbi.nlm.nih.gov/pubmed/29593876
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omx108
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