Rendú Osler Weber Syndrome; case report()

Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber disease, is a dominant autosomal disease characterized by the presence of multiple telangiectasia in skin and mucus, associated with arteriovenous malformations (AVM) of various organs, including the lungs, gastrointestinal system and...

Descripción completa

Detalles Bibliográficos
Autores principales: García Córdova, Oscar Manuel, Pérez Morales, Tania Cristina, Barón Hernández, Verónica Andrea del Pilar, Cuéllar, José Sebastián Sotelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214720/
https://www.ncbi.nlm.nih.gov/pubmed/35755112
http://dx.doi.org/10.1016/j.radcr.2022.05.088

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214720/
https://www.ncbi.nlm.nih.gov/pubmed/35755112
http://dx.doi.org/10.1016/j.radcr.2022.05.088

Ejemplares similares