A Rare Case of Hereditary Hemorrhagic Telangiectasia: A Case Report

Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is a very rare autosomal dominant genetic disorder that leads to abnormal blood vessel formation in the skin, mucus membranes (called telangiectasia), and organs such as the lung, liver, and brain. It occurs due t...

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Detalles Bibliográficos
Autores principales: Khan, Ahmad R., Waqar, Salma, Wazir, Muhammad Hayyan, Arif, Amina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136551/
https://www.ncbi.nlm.nih.gov/pubmed/35651452
http://dx.doi.org/10.7759/cureus.24517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136551/
https://www.ncbi.nlm.nih.gov/pubmed/35651452
http://dx.doi.org/10.7759/cureus.24517

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