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Hereditary Hemorrhagic Telangiectasia: A Rare Cause of Anemia
Hereditary hemorrhagic telangiectasias (HHT), also known as Osler-Weber-Rendu syndrome, is an uncommon genetic disorder. It is inherited as an autosomal dominant disorder with varying penetrance and expression. The diagnosis of HHT requires the presence of at least three out of four clinical criteri...
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| Publicat a: | Cureus |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Cureus
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6779147/ https://ncbi.nlm.nih.gov/pubmed/31602353 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.5349 |
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