Imaging of Heritable Thoracic Aortic Disease
Heritable Thoracic Aortic Disease (HTAD) is caused by mutation of a gene that confers a high risk for thoracic aortic aneurysms and dissections. Syndromic HTAD are associated with systemic manifestations and include Marfan, Loeys-Dietz, vascular Ehlers Danlos and Turner Syndromes. The purpose of thi...
Gespeichert in:
| Veröffentlicht in: | Seminars in roentgenology 2022-10, Vol.57 (4), p.364-379 |
|---|---|
| Hauptverfasser: | , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 379 |
|---|---|
| container_issue | 4 |
| container_start_page | 364 |
| container_title | Seminars in roentgenology |
| container_volume | 57 |
| creator | Tijmes, Felipe Sanchez Karur, Gauri Rani |
| description | Heritable Thoracic Aortic Disease (HTAD) is caused by mutation of a gene that confers a high risk for thoracic aortic aneurysms and dissections. Syndromic HTAD are associated with systemic manifestations and include Marfan, Loeys-Dietz, vascular Ehlers Danlos and Turner Syndromes. The purpose of this review is to summarize the pathophysiology, cardiovascular imaging features and management of HTAD. Imaging plays an important role in screening for aortic dilatation and monitoring progression. Echocardiogram, Computed tomography and Magnetic resonance imaging are the commonly used modalities. Based on consensus guidelines, prophylactic aortic replacement is indicated when a certain threshold diameter is reached. |
| doi_str_mv | 10.1053/j.ro.2022.07.004 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2727645202</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0037198X22000451</els_id><sourcerecordid>2727645202</sourcerecordid><originalsourceid>FETCH-LOGICAL-c327t-bfd10b981ed7d7ae365aa11938625f6e5367a547b19e7d5e1df47b5183b5044e3</originalsourceid><addsrcrecordid>eNp1kM9LwzAYhoMoOKd3jz16sPVL0iSttzF_bDDwMsFbSNOvM6NdZtIJ_vdmzKunlw_e54P3IeSWQkFB8IdtEXzBgLECVAFQnpEJFaLKSymqczIB4CqndfVxSa5i3AKwWlI6IffLwWzcbpP5LltgcKNpeszWnz4Y62w282FM8eQimojX5KIzfcSbv5yS95fn9XyRr95el_PZKrecqTFvupZCU1cUW9Uqg1wKYyiteSWZ6CQKLpURpWpojaoVSNsuHYJWvBFQlsin5O70dx_81wHjqAcXLfa92aE_RM0UU7IUaW2qwqlqg48xYKf3wQ0m_GgK-ihGb3Xw-ihGg9JJTEIeTwimCd8Og47W4c5i6wLaUbfe_Q__AgqiaLc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2727645202</pqid></control><display><type>article</type><title>Imaging of Heritable Thoracic Aortic Disease</title><source>ScienceDirect Journals (5 years ago - present)</source><creator>Tijmes, Felipe Sanchez ; Karur, Gauri Rani</creator><creatorcontrib>Tijmes, Felipe Sanchez ; Karur, Gauri Rani</creatorcontrib><description>Heritable Thoracic Aortic Disease (HTAD) is caused by mutation of a gene that confers a high risk for thoracic aortic aneurysms and dissections. Syndromic HTAD are associated with systemic manifestations and include Marfan, Loeys-Dietz, vascular Ehlers Danlos and Turner Syndromes. The purpose of this review is to summarize the pathophysiology, cardiovascular imaging features and management of HTAD. Imaging plays an important role in screening for aortic dilatation and monitoring progression. Echocardiogram, Computed tomography and Magnetic resonance imaging are the commonly used modalities. Based on consensus guidelines, prophylactic aortic replacement is indicated when a certain threshold diameter is reached.</description><identifier>ISSN: 0037-198X</identifier><identifier>EISSN: 1558-4658</identifier><identifier>DOI: 10.1053/j.ro.2022.07.004</identifier><language>eng</language><publisher>Elsevier Inc</publisher><ispartof>Seminars in roentgenology, 2022-10, Vol.57 (4), p.364-379</ispartof><rights>2022 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-bfd10b981ed7d7ae365aa11938625f6e5367a547b19e7d5e1df47b5183b5044e3</citedby><cites>FETCH-LOGICAL-c327t-bfd10b981ed7d7ae365aa11938625f6e5367a547b19e7d5e1df47b5183b5044e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1053/j.ro.2022.07.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids></links><search><creatorcontrib>Tijmes, Felipe Sanchez</creatorcontrib><creatorcontrib>Karur, Gauri Rani</creatorcontrib><title>Imaging of Heritable Thoracic Aortic Disease</title><title>Seminars in roentgenology</title><description>Heritable Thoracic Aortic Disease (HTAD) is caused by mutation of a gene that confers a high risk for thoracic aortic aneurysms and dissections. Syndromic HTAD are associated with systemic manifestations and include Marfan, Loeys-Dietz, vascular Ehlers Danlos and Turner Syndromes. The purpose of this review is to summarize the pathophysiology, cardiovascular imaging features and management of HTAD. Imaging plays an important role in screening for aortic dilatation and monitoring progression. Echocardiogram, Computed tomography and Magnetic resonance imaging are the commonly used modalities. Based on consensus guidelines, prophylactic aortic replacement is indicated when a certain threshold diameter is reached.</description><issn>0037-198X</issn><issn>1558-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kM9LwzAYhoMoOKd3jz16sPVL0iSttzF_bDDwMsFbSNOvM6NdZtIJ_vdmzKunlw_e54P3IeSWQkFB8IdtEXzBgLECVAFQnpEJFaLKSymqczIB4CqndfVxSa5i3AKwWlI6IffLwWzcbpP5LltgcKNpeszWnz4Y62w282FM8eQimojX5KIzfcSbv5yS95fn9XyRr95el_PZKrecqTFvupZCU1cUW9Uqg1wKYyiteSWZ6CQKLpURpWpojaoVSNsuHYJWvBFQlsin5O70dx_81wHjqAcXLfa92aE_RM0UU7IUaW2qwqlqg48xYKf3wQ0m_GgK-ihGb3Xw-ihGg9JJTEIeTwimCd8Og47W4c5i6wLaUbfe_Q__AgqiaLc</recordid><startdate>202210</startdate><enddate>202210</enddate><creator>Tijmes, Felipe Sanchez</creator><creator>Karur, Gauri Rani</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202210</creationdate><title>Imaging of Heritable Thoracic Aortic Disease</title><author>Tijmes, Felipe Sanchez ; Karur, Gauri Rani</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-bfd10b981ed7d7ae365aa11938625f6e5367a547b19e7d5e1df47b5183b5044e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tijmes, Felipe Sanchez</creatorcontrib><creatorcontrib>Karur, Gauri Rani</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Seminars in roentgenology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tijmes, Felipe Sanchez</au><au>Karur, Gauri Rani</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Imaging of Heritable Thoracic Aortic Disease</atitle><jtitle>Seminars in roentgenology</jtitle><date>2022-10</date><risdate>2022</risdate><volume>57</volume><issue>4</issue><spage>364</spage><epage>379</epage><pages>364-379</pages><issn>0037-198X</issn><eissn>1558-4658</eissn><abstract>Heritable Thoracic Aortic Disease (HTAD) is caused by mutation of a gene that confers a high risk for thoracic aortic aneurysms and dissections. Syndromic HTAD are associated with systemic manifestations and include Marfan, Loeys-Dietz, vascular Ehlers Danlos and Turner Syndromes. The purpose of this review is to summarize the pathophysiology, cardiovascular imaging features and management of HTAD. Imaging plays an important role in screening for aortic dilatation and monitoring progression. Echocardiogram, Computed tomography and Magnetic resonance imaging are the commonly used modalities. Based on consensus guidelines, prophylactic aortic replacement is indicated when a certain threshold diameter is reached.</abstract><pub>Elsevier Inc</pub><doi>10.1053/j.ro.2022.07.004</doi><tpages>16</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0037-198X |
| ispartof | Seminars in roentgenology, 2022-10, Vol.57 (4), p.364-379 |
| issn | 0037-198X 1558-4658 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_2727645202 |
| source | ScienceDirect Journals (5 years ago - present) |
| title | Imaging of Heritable Thoracic Aortic Disease |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T18%3A14%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Imaging%20of%20Heritable%20Thoracic%20Aortic%20Disease&rft.jtitle=Seminars%20in%20roentgenology&rft.au=Tijmes,%20Felipe%20Sanchez&rft.date=2022-10&rft.volume=57&rft.issue=4&rft.spage=364&rft.epage=379&rft.pages=364-379&rft.issn=0037-198X&rft.eissn=1558-4658&rft_id=info:doi/10.1053/j.ro.2022.07.004&rft_dat=%3Cproquest_cross%3E2727645202%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2727645202&rft_id=info:pmid/&rft_els_id=S0037198X22000451&rfr_iscdi=true |