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A challenging case of anemia, respiratory failure and seizures
BACKGROUND. Hemorrhagic Hereditary Telangiectasia (HHT), or Rendu-Osler-Weber syndrome, is a rare genetic disorder characterized by mucocutaneous telangiectasias and visceral arteriovenous malformations. AIM AND METHODS. We describe the case of a 64-year old woman in which a multidisciplinary evalua...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Mattioli 1885
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510998/ https://www.ncbi.nlm.nih.gov/pubmed/36129446 http://dx.doi.org/10.23750/abm.v93iS1.13076 |