Integration of clinical parameters, genotype and epistaxis severity score to guide treatment for hereditary hemorrhagic telangiectasia associated bleeding

BACKGROUND: Hereditary Hemorrhagic Telangiectasia (HHT) is a rare inherited disorder characterized by development of mucocutaneous telangiectases and visceral organ arteriovenous malformations, which can lead to recurrent, spontaneous bleeding and development of iron deficiency anemia. The primary o...

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Detalles Bibliográficos
Autores principales: Beckman, Joan D., Li, Quefeng, Hester, Samuel T., Leitner, Ofri, Smith, Karen L., Kasthuri, Raj S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359017/
https://www.ncbi.nlm.nih.gov/pubmed/32660636
http://dx.doi.org/10.1186/s13023-020-01453-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359017/
https://www.ncbi.nlm.nih.gov/pubmed/32660636
http://dx.doi.org/10.1186/s13023-020-01453-1

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