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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...
Tallennettuna:
| Julkaisussa: | Cureus |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Cureus
2019
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| Aiheet: | |
| Linkit: | 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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