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Imaging to intervention: a review of what the Interventionalist needs to Know about Hereditary Hemorrhagic Telangiectasia

dc.contributor.authorSobrepera, Stephanie
dc.contributor.authorMonroe, Eric
dc.contributor.authorGemmete, Joseph J.
dc.contributor.authorHallam, Danial
dc.contributor.authorPinchot, Jason W.
dc.contributor.authorKaufman, Claire
dc.date.accessioned2022-08-10T18:55:05Z
dc.date.available2022-08-10T18:55:05Z
dc.date.issued2021-12-09
dc.identifier.citationCVIR Endovascular. 2021 Dec 09;4(1):84
dc.identifier.urihttps://doi.org/10.1186/s42155-021-00270-2
dc.identifier.urihttps://hdl.handle.net/2027.42/174065en
dc.description.abstractAbstract Hereditary hemorrhagic telangiectasia (HHT) is a disorder that affects 1 in 5000–10,000 people worldwide and can result in devastating complications such as cerebral abscess, stroke, massive hemorrhage, and even death. HHT is an autosomal dominant disorder that leads to the formation of abnormal communication between the arteries and veins with a resultant spectrum of vascular anomalies. The disorder affects many organ systems and thus requires a dedicated multidisciplinary approach. Interventional radiologists are vital members of this team providing expertise not only in disease management, but in complex embolotherapy, helping to maintain the health of these patients. This article reviews clinical manifestations, screening guidelines, diagnostic criteria, and endovascular management of HHT.
dc.titleImaging to intervention: a review of what the Interventionalist needs to Know about Hereditary Hemorrhagic Telangiectasia
dc.typeJournal Article
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/174065/1/42155_2021_Article_270.pdf
dc.identifier.doihttps://dx.doi.org/10.7302/5796
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dc.date.updated2022-08-10T18:55:04Z
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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