Diagnosis and Management of Constitutional Mismatch Repair Deficiency Syndrome

Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder that has little more than 200 total cases reported as of 2020. Whereas a single mutation in genes responsible for mismatch repair causes the autosomal dominant Lynch syndrome (LS), CMMRD is caus...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The American surgeon 2023-09, Vol.89 (9), p.3953-3955
Hauptverfasser: Winter, Kelly, Tan, Martin, Briscoe, Eric, Hyde, Alan, Daniel Stanley, J.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3955
container_issue 9
container_start_page 3953
container_title The American surgeon
container_volume 89
creator Winter, Kelly
Tan, Martin
Briscoe, Eric
Hyde, Alan
Daniel Stanley, J.
description Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder that has little more than 200 total cases reported as of 2020. Whereas a single mutation in genes responsible for mismatch repair causes the autosomal dominant Lynch syndrome (LS), CMMRD is caused by biallelic heterozygous defects: distinct deleterious mutations on each allele for a single gene. As the disease is exceedingly rare and may present via a wide variety of signs, including neurofibromatosis type 1- and Lynch Syndrome-associated malignancies, diagnosis and subsequent surveillance are complex with suggested methods published by the International Replication Repair Deficiency Consortium. We report here the history and management of a patient whose newly diagnosed CMMRD was managed with both curative and prophylactic surgical treatment.
doi_str_mv 10.1177/00031348231173987
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2821643727</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_00031348231173987</sage_id><sourcerecordid>2821643727</sourcerecordid><originalsourceid>FETCH-LOGICAL-c292t-c2bc66758975bee8994f9f2f798abde83ed52a785d1717beefab5a9a07933f133</originalsourceid><addsrcrecordid>eNp9kMtOwzAQRS0EoqXwAWyQl2xS_Ihje4laXlILEo915CR2cZXYxU4W_XtctbBBYjOjsc9caQ4AlxhNMeb8BiFEMc0FoWmkUvAjMMaMsUymp2Mw3v1nO2AEzmJcpzEvGD4FI8pJgZDMx-B5btXK-WgjVK6BS-XUSnfa9dAbOPMu9rYfeuudauHSxk719Sd81RtlA5xrY2urXb2Fb1vXBN_pc3BiVBv1xaFPwMf93fvsMVu8PDzNbhdZTSTpU63qouBMSM4qrYWUuZGGGC6FqhotqG4YUVywBnPME2FUxZRUiEtKDaZ0Aq73uZvgvwYd-7KzsdZtq5z2QyyJILjI05k8oXiP1sHHGLQpN8F2KmxLjMqdxvKPxrRzdYgfqk43vxs_3hIw3QMx6SrXfghJUPwn8RuRYXpp</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2821643727</pqid></control><display><type>article</type><title>Diagnosis and Management of Constitutional Mismatch Repair Deficiency Syndrome</title><source>Access via SAGE</source><creator>Winter, Kelly ; Tan, Martin ; Briscoe, Eric ; Hyde, Alan ; Daniel Stanley, J.</creator><creatorcontrib>Winter, Kelly ; Tan, Martin ; Briscoe, Eric ; Hyde, Alan ; Daniel Stanley, J.</creatorcontrib><description>Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder that has little more than 200 total cases reported as of 2020. Whereas a single mutation in genes responsible for mismatch repair causes the autosomal dominant Lynch syndrome (LS), CMMRD is caused by biallelic heterozygous defects: distinct deleterious mutations on each allele for a single gene. As the disease is exceedingly rare and may present via a wide variety of signs, including neurofibromatosis type 1- and Lynch Syndrome-associated malignancies, diagnosis and subsequent surveillance are complex with suggested methods published by the International Replication Repair Deficiency Consortium. We report here the history and management of a patient whose newly diagnosed CMMRD was managed with both curative and prophylactic surgical treatment.</description><identifier>ISSN: 0003-1348</identifier><identifier>EISSN: 1555-9823</identifier><identifier>DOI: 10.1177/00031348231173987</identifier><identifier>PMID: 37260094</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><ispartof>The American surgeon, 2023-09, Vol.89 (9), p.3953-3955</ispartof><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c292t-c2bc66758975bee8994f9f2f798abde83ed52a785d1717beefab5a9a07933f133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/00031348231173987$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/00031348231173987$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>315,781,785,21824,27929,27930,43626,43627</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37260094$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Winter, Kelly</creatorcontrib><creatorcontrib>Tan, Martin</creatorcontrib><creatorcontrib>Briscoe, Eric</creatorcontrib><creatorcontrib>Hyde, Alan</creatorcontrib><creatorcontrib>Daniel Stanley, J.</creatorcontrib><title>Diagnosis and Management of Constitutional Mismatch Repair Deficiency Syndrome</title><title>The American surgeon</title><addtitle>Am Surg</addtitle><description>Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder that has little more than 200 total cases reported as of 2020. Whereas a single mutation in genes responsible for mismatch repair causes the autosomal dominant Lynch syndrome (LS), CMMRD is caused by biallelic heterozygous defects: distinct deleterious mutations on each allele for a single gene. As the disease is exceedingly rare and may present via a wide variety of signs, including neurofibromatosis type 1- and Lynch Syndrome-associated malignancies, diagnosis and subsequent surveillance are complex with suggested methods published by the International Replication Repair Deficiency Consortium. We report here the history and management of a patient whose newly diagnosed CMMRD was managed with both curative and prophylactic surgical treatment.</description><issn>0003-1348</issn><issn>1555-9823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EoqXwAWyQl2xS_Ihje4laXlILEo915CR2cZXYxU4W_XtctbBBYjOjsc9caQ4AlxhNMeb8BiFEMc0FoWmkUvAjMMaMsUymp2Mw3v1nO2AEzmJcpzEvGD4FI8pJgZDMx-B5btXK-WgjVK6BS-XUSnfa9dAbOPMu9rYfeuudauHSxk719Sd81RtlA5xrY2urXb2Fb1vXBN_pc3BiVBv1xaFPwMf93fvsMVu8PDzNbhdZTSTpU63qouBMSM4qrYWUuZGGGC6FqhotqG4YUVywBnPME2FUxZRUiEtKDaZ0Aq73uZvgvwYd-7KzsdZtq5z2QyyJILjI05k8oXiP1sHHGLQpN8F2KmxLjMqdxvKPxrRzdYgfqk43vxs_3hIw3QMx6SrXfghJUPwn8RuRYXpp</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Winter, Kelly</creator><creator>Tan, Martin</creator><creator>Briscoe, Eric</creator><creator>Hyde, Alan</creator><creator>Daniel Stanley, J.</creator><general>SAGE Publications</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20230901</creationdate><title>Diagnosis and Management of Constitutional Mismatch Repair Deficiency Syndrome</title><author>Winter, Kelly ; Tan, Martin ; Briscoe, Eric ; Hyde, Alan ; Daniel Stanley, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c292t-c2bc66758975bee8994f9f2f798abde83ed52a785d1717beefab5a9a07933f133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Winter, Kelly</creatorcontrib><creatorcontrib>Tan, Martin</creatorcontrib><creatorcontrib>Briscoe, Eric</creatorcontrib><creatorcontrib>Hyde, Alan</creatorcontrib><creatorcontrib>Daniel Stanley, J.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The American surgeon</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Winter, Kelly</au><au>Tan, Martin</au><au>Briscoe, Eric</au><au>Hyde, Alan</au><au>Daniel Stanley, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnosis and Management of Constitutional Mismatch Repair Deficiency Syndrome</atitle><jtitle>The American surgeon</jtitle><addtitle>Am Surg</addtitle><date>2023-09-01</date><risdate>2023</risdate><volume>89</volume><issue>9</issue><spage>3953</spage><epage>3955</epage><pages>3953-3955</pages><issn>0003-1348</issn><eissn>1555-9823</eissn><abstract>Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder that has little more than 200 total cases reported as of 2020. Whereas a single mutation in genes responsible for mismatch repair causes the autosomal dominant Lynch syndrome (LS), CMMRD is caused by biallelic heterozygous defects: distinct deleterious mutations on each allele for a single gene. As the disease is exceedingly rare and may present via a wide variety of signs, including neurofibromatosis type 1- and Lynch Syndrome-associated malignancies, diagnosis and subsequent surveillance are complex with suggested methods published by the International Replication Repair Deficiency Consortium. We report here the history and management of a patient whose newly diagnosed CMMRD was managed with both curative and prophylactic surgical treatment.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>37260094</pmid><doi>10.1177/00031348231173987</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0003-1348
ispartof The American surgeon, 2023-09, Vol.89 (9), p.3953-3955
issn 0003-1348
1555-9823
language eng
recordid cdi_proquest_miscellaneous_2821643727
source Access via SAGE
title Diagnosis and Management of Constitutional Mismatch Repair Deficiency Syndrome
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T23%3A46%3A54IST&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=Diagnosis%20and%20Management%20of%20Constitutional%20Mismatch%20Repair%20Deficiency%20Syndrome&rft.jtitle=The%20American%20surgeon&rft.au=Winter,%20Kelly&rft.date=2023-09-01&rft.volume=89&rft.issue=9&rft.spage=3953&rft.epage=3955&rft.pages=3953-3955&rft.issn=0003-1348&rft.eissn=1555-9823&rft_id=info:doi/10.1177/00031348231173987&rft_dat=%3Cproquest_cross%3E2821643727%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=2821643727&rft_id=info:pmid/37260094&rft_sage_id=10.1177_00031348231173987&rfr_iscdi=true