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...

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Detalles Bibliográficos
Autores principales: Bova, Carlo, De Bartolo, Tommaso, De Stefano, Roberto, Ruvio, Martina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2022
Materias:
Case Report
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

Internet

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

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