Case report: Diagnosis of hereditary hemorrhagic telangiectasia (Osler Weber Rendu Syndrome) in a 23-year-old male presented with anemia and thrombocytopenia and its response to bevacizumab

Osler Weber Rendu Syndrome (OWS) is characterized by the development of abnormally dilated blood vessels, which manifest as arteriovenous shunts (pulmonary, gastrointestinal, hepatic, and cerebral) and mucocutaneous telangiectasias (lips, tongue, and fingertips). It is an autosomal dominant disease...

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Detalles Bibliográficos
Autores principales: Yunus, Hamza, Amin, Said, Haq, Furqan Ul, Ali, Waqar, Hamid, Tanveer, Ali, Wajid, Ullah, Basharat, Bai, Payal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575171/
https://www.ncbi.nlm.nih.gov/pubmed/36262274
http://dx.doi.org/10.3389/fmed.2022.1001695

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575171/
https://www.ncbi.nlm.nih.gov/pubmed/36262274
http://dx.doi.org/10.3389/fmed.2022.1001695

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