Loading…
A rare case of arterial tortuosity syndrome in an adult
Arterial tortuosity syndrome (ATS) is rare autosomal recessive connective tissue disorder. It affects large and medium-sized arteries inducing tortuosity and elongation. Typical skeletal manifestations are dysmorphic features, hyperextensible skin, hypermobile joints, and congenital contractures. We...
Saved in:
| Published in: | Radiology case reports 2022-08, Vol.17 (8), p.2594-2597 |
|---|---|
| Main Authors: | , , , , |
| Format: | Article |
| Language: | English |
| Subjects: | |
| Citations: | Items that this one cites |
| Online Access: | Get full text |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| cited_by | |
|---|---|
| cites | cdi_FETCH-LOGICAL-c2875-439fbf153c57ba8d2632becae0228c083aa65266bdebd4f2dfb1b7d04eb741a83 |
| container_end_page | 2597 |
| container_issue | 8 |
| container_start_page | 2594 |
| container_title | Radiology case reports |
| container_volume | 17 |
| creator | Elnaggar, Mohamed Elsayed Aly, Mahmoud Mohamed Abduljawad, Hiba Bubshait, Maryam Ebrahim, Wael Hamed |
| description | Arterial tortuosity syndrome (ATS) is rare autosomal recessive connective tissue disorder. It affects large and medium-sized arteries inducing tortuosity and elongation. Typical skeletal manifestations are dysmorphic features, hyperextensible skin, hypermobile joints, and congenital contractures.
We present a case of a 33-year-old female, with history of multiple abdominal wall hernias, who was diagnosed with ATS by preoperative investigations based on typical vascular manifestations. We will present the radiological findings of this rare condition. |
| doi_str_mv | 10.1016/j.radcr.2022.05.005 |
| format | article |
| fullrecord | <record><control><sourceid>elsevier_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_11de34d03d0e49f79239e4e53b907f4c</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1930043322003508</els_id><doaj_id>oai_doaj_org_article_11de34d03d0e49f79239e4e53b907f4c</doaj_id><sourcerecordid>S1930043322003508</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2875-439fbf153c57ba8d2632becae0228c083aa65266bdebd4f2dfb1b7d04eb741a83</originalsourceid><addsrcrecordid>eNp9kUtqHDEQhkVIiB_JCQymLzDt0qsfiwSMSWyDIZtkLUpSydHQ0zJSj2Fuk7PkZNF4EmNvsqqiqv6vSvoZO-PQcuDdxbrN6F1uBQjRgm4B9Bt2zEcJK1BSvn2RH7GTUtYAnRx6_p4dSd3VFPQxGy6bjJkah4WaFBrMC-WIU7OkvGxTicuuKbvZ57ShJs4Nzr9_od9Oywf2LuBU6OPfeMp-fP3y_epmdfft-vbq8m7lxNDrlZJjsIFr6XRvcfCik8KSQ6pHDw4Gidhp0XXWk_UqCB8st70HRbZXHAd5ym4PXJ9wbR5y3GDemYTRPBVSvjf15ugmMpx7ksqD9EBqDP0o5EiKtLQj9EG5yvp8YD1s7Ya8o3nJOL2Cvu7M8ae5T49m5Lrng6oAeQC4nErJFJ61HMzeFLM2T6aYvSkGtKmmVNX5y7XPmn8u1IFPhwGqH_kYKZviIs2OfMzklvrS-N8FfwAMnqA4</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A rare case of arterial tortuosity syndrome in an adult</title><source>PubMed (Medline)</source><source>Elsevier ScienceDirect Journals</source><creator>Elnaggar, Mohamed Elsayed ; Aly, Mahmoud Mohamed ; Abduljawad, Hiba ; Bubshait, Maryam ; Ebrahim, Wael Hamed</creator><creatorcontrib>Elnaggar, Mohamed Elsayed ; Aly, Mahmoud Mohamed ; Abduljawad, Hiba ; Bubshait, Maryam ; Ebrahim, Wael Hamed</creatorcontrib><description>Arterial tortuosity syndrome (ATS) is rare autosomal recessive connective tissue disorder. It affects large and medium-sized arteries inducing tortuosity and elongation. Typical skeletal manifestations are dysmorphic features, hyperextensible skin, hypermobile joints, and congenital contractures.
We present a case of a 33-year-old female, with history of multiple abdominal wall hernias, who was diagnosed with ATS by preoperative investigations based on typical vascular manifestations. We will present the radiological findings of this rare condition.</description><identifier>ISSN: 1930-0433</identifier><identifier>EISSN: 1930-0433</identifier><identifier>DOI: 10.1016/j.radcr.2022.05.005</identifier><identifier>PMID: 35663805</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Arterial tortuosity syndrome ; Case Report ; Mandering vessel sign ; V sign</subject><ispartof>Radiology case reports, 2022-08, Vol.17 (8), p.2594-2597</ispartof><rights>2022</rights><rights>2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington.</rights><rights>2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2875-439fbf153c57ba8d2632becae0228c083aa65266bdebd4f2dfb1b7d04eb741a83</cites><orcidid>0000-0002-8356-0112 ; 0000-0003-0600-0717 ; 0000-0002-8326-4495</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157184/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1930043322003508$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3549,27924,27925,45780,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35663805$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Elnaggar, Mohamed Elsayed</creatorcontrib><creatorcontrib>Aly, Mahmoud Mohamed</creatorcontrib><creatorcontrib>Abduljawad, Hiba</creatorcontrib><creatorcontrib>Bubshait, Maryam</creatorcontrib><creatorcontrib>Ebrahim, Wael Hamed</creatorcontrib><title>A rare case of arterial tortuosity syndrome in an adult</title><title>Radiology case reports</title><addtitle>Radiol Case Rep</addtitle><description>Arterial tortuosity syndrome (ATS) is rare autosomal recessive connective tissue disorder. It affects large and medium-sized arteries inducing tortuosity and elongation. Typical skeletal manifestations are dysmorphic features, hyperextensible skin, hypermobile joints, and congenital contractures.
We present a case of a 33-year-old female, with history of multiple abdominal wall hernias, who was diagnosed with ATS by preoperative investigations based on typical vascular manifestations. We will present the radiological findings of this rare condition.</description><subject>Arterial tortuosity syndrome</subject><subject>Case Report</subject><subject>Mandering vessel sign</subject><subject>V sign</subject><issn>1930-0433</issn><issn>1930-0433</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kUtqHDEQhkVIiB_JCQymLzDt0qsfiwSMSWyDIZtkLUpSydHQ0zJSj2Fuk7PkZNF4EmNvsqqiqv6vSvoZO-PQcuDdxbrN6F1uBQjRgm4B9Bt2zEcJK1BSvn2RH7GTUtYAnRx6_p4dSd3VFPQxGy6bjJkah4WaFBrMC-WIU7OkvGxTicuuKbvZ57ShJs4Nzr9_od9Oywf2LuBU6OPfeMp-fP3y_epmdfft-vbq8m7lxNDrlZJjsIFr6XRvcfCik8KSQ6pHDw4Gidhp0XXWk_UqCB8st70HRbZXHAd5ym4PXJ9wbR5y3GDemYTRPBVSvjf15ugmMpx7ksqD9EBqDP0o5EiKtLQj9EG5yvp8YD1s7Ya8o3nJOL2Cvu7M8ae5T49m5Lrng6oAeQC4nErJFJ61HMzeFLM2T6aYvSkGtKmmVNX5y7XPmn8u1IFPhwGqH_kYKZviIs2OfMzklvrS-N8FfwAMnqA4</recordid><startdate>202208</startdate><enddate>202208</enddate><creator>Elnaggar, Mohamed Elsayed</creator><creator>Aly, Mahmoud Mohamed</creator><creator>Abduljawad, Hiba</creator><creator>Bubshait, Maryam</creator><creator>Ebrahim, Wael Hamed</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-8356-0112</orcidid><orcidid>https://orcid.org/0000-0003-0600-0717</orcidid><orcidid>https://orcid.org/0000-0002-8326-4495</orcidid></search><sort><creationdate>202208</creationdate><title>A rare case of arterial tortuosity syndrome in an adult</title><author>Elnaggar, Mohamed Elsayed ; Aly, Mahmoud Mohamed ; Abduljawad, Hiba ; Bubshait, Maryam ; Ebrahim, Wael Hamed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2875-439fbf153c57ba8d2632becae0228c083aa65266bdebd4f2dfb1b7d04eb741a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Arterial tortuosity syndrome</topic><topic>Case Report</topic><topic>Mandering vessel sign</topic><topic>V sign</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elnaggar, Mohamed Elsayed</creatorcontrib><creatorcontrib>Aly, Mahmoud Mohamed</creatorcontrib><creatorcontrib>Abduljawad, Hiba</creatorcontrib><creatorcontrib>Bubshait, Maryam</creatorcontrib><creatorcontrib>Ebrahim, Wael Hamed</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Radiology case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elnaggar, Mohamed Elsayed</au><au>Aly, Mahmoud Mohamed</au><au>Abduljawad, Hiba</au><au>Bubshait, Maryam</au><au>Ebrahim, Wael Hamed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A rare case of arterial tortuosity syndrome in an adult</atitle><jtitle>Radiology case reports</jtitle><addtitle>Radiol Case Rep</addtitle><date>2022-08</date><risdate>2022</risdate><volume>17</volume><issue>8</issue><spage>2594</spage><epage>2597</epage><pages>2594-2597</pages><issn>1930-0433</issn><eissn>1930-0433</eissn><abstract>Arterial tortuosity syndrome (ATS) is rare autosomal recessive connective tissue disorder. It affects large and medium-sized arteries inducing tortuosity and elongation. Typical skeletal manifestations are dysmorphic features, hyperextensible skin, hypermobile joints, and congenital contractures.
We present a case of a 33-year-old female, with history of multiple abdominal wall hernias, who was diagnosed with ATS by preoperative investigations based on typical vascular manifestations. We will present the radiological findings of this rare condition.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>35663805</pmid><doi>10.1016/j.radcr.2022.05.005</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-8356-0112</orcidid><orcidid>https://orcid.org/0000-0003-0600-0717</orcidid><orcidid>https://orcid.org/0000-0002-8326-4495</orcidid><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1930-0433 |
| ispartof | Radiology case reports, 2022-08, Vol.17 (8), p.2594-2597 |
| issn | 1930-0433 1930-0433 |
| language | eng |
| recordid | cdi_doaj_primary_oai_doaj_org_article_11de34d03d0e49f79239e4e53b907f4c |
| source | PubMed (Medline); Elsevier ScienceDirect Journals |
| subjects | Arterial tortuosity syndrome Case Report Mandering vessel sign V sign |
| title | A rare case of arterial tortuosity syndrome in an adult |
| url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T07%3A09%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20rare%20case%20of%20arterial%20tortuosity%20syndrome%20in%20an%C2%A0adult&rft.jtitle=Radiology%20case%20reports&rft.au=Elnaggar,%20Mohamed%20Elsayed&rft.date=2022-08&rft.volume=17&rft.issue=8&rft.spage=2594&rft.epage=2597&rft.pages=2594-2597&rft.issn=1930-0433&rft.eissn=1930-0433&rft_id=info:doi/10.1016/j.radcr.2022.05.005&rft_dat=%3Celsevier_doaj_%3ES1930043322003508%3C/elsevier_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2875-439fbf153c57ba8d2632becae0228c083aa65266bdebd4f2dfb1b7d04eb741a83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/35663805&rfr_iscdi=true |