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Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations

Hereditary haemorrhagic telangiectasia (HHT) also known as Osler-Weber-Rendu syndrome is an autosomal dominant disorder affecting 1 in 8000 individuals. The eponym recognises the 19th-century physicians William Osler, Henri Jules Louis Marie Rendu and Frederick Parkes Weber who each independently de...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMJ Case Rep
Egile Nagusiak: Dunphy, Louise, Talwar, Ambika, Patel, Neil, Evans, Alex
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BMJ Publishing Group 2021
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7799076/
https://ncbi.nlm.nih.gov/pubmed/33419752
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2020-238385
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