Pancytopenia in a Patient with Rendu-Osler-Weber Syndrome and Uncommon Vascular Abnormalities

Rendu-Osler-Weber syndrome, or hereditary hemorrhagic teleangiectasia (HHT), is a rare autosomal dominant vascular disorder, characterized by multiple mucocutaneous teleangiectases with recurrent nasal and gastrointestinal bleedings and/or solid-organ arteriovenous shunts. We describe the first case...

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Detalles Bibliográficos
Autores principales: Binello, Nicolò, Gasbarrini, Antonio, Gaetani, Eleonora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075613/
https://www.ncbi.nlm.nih.gov/pubmed/27803822
http://dx.doi.org/10.1155/2016/3016402

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075613/
https://www.ncbi.nlm.nih.gov/pubmed/27803822
http://dx.doi.org/10.1155/2016/3016402

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