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Visceral manifestations in hereditary haemorrhagic telangiectasia type 2
Hereditary haemorrhagic telangiectasia (HHT) is a genetic vascular disorder characterised by epistaxis, telangiectases, and visceral manifestations. The two known disease types, HHT1 and HHT2, are caused by mutations in the endoglin (ENG) and ALK-1 genes, respectively. A higher frequency of pulmonar...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735537/ https://ncbi.nlm.nih.gov/pubmed/12843319 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.40.7.494 |
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