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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...
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| Pubblicato in: | BMJ Case Rep |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMJ Publishing Group
2021
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| Soggetti: | |
| Accesso online: | 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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