{"id":205,"date":"2015-04-13T13:51:40","date_gmt":"2015-04-13T13:51:40","guid":{"rendered":"https:\/\/primarycaregenetics.eshg.org\/?page_id=205"},"modified":"2016-01-10T11:21:08","modified_gmt":"2016-01-10T11:21:08","slug":"red-flags","status":"publish","type":"page","link":"https:\/\/www.primarycaregenetics.org\/?page_id=205&lang=en","title":{"rendered":"Red flags"},"content":{"rendered":"<p>In many clinical situations where there is a significant risk of a genetic condition, certain red flags will alert you as a professional to look further.<\/p>\n<p>For example, when a patient asks about a family history of cancer, significant history would include:<\/p>\n<ul>\n<li>relatives who were affected by cancer at a younger age than you would expect<\/li>\n<li>relatives with cancers that could be part of a cancer syndrome (such as breast and ovarian cancer, or colon and endometrial cancer)<\/li>\n<li>multiple primaries in the same person<\/li>\n<li>unusual cancers, such as breast cancer in a male.<\/li>\n<\/ul>\n<p>In each of our modules, we will cover \u2018red flag\u2019 situations to help you identify patients at risk.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>In many clinical situations where there is a significant risk of a genetic condition, certain red flags will alert you as a professional to look further. For example, when a patient asks about a family history of cancer, significant history would include: relatives who were affected by cancer at a younger age than you would expect relatives with cancers that could be part of a cancer syndrome (such as breast and ovarian cancer, or colon and endometrial cancer) multiple primaries [&#8230;]<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":0,"menu_order":57,"comment_status":"closed","ping_status":"closed","template":"template-fullwidth.php","meta":{"ngg_post_thumbnail":0},"_links":{"self":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/205"}],"collection":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=205"}],"version-history":[{"count":2,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/205\/revisions"}],"predecessor-version":[{"id":293,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/205\/revisions\/293"}],"wp:attachment":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=205"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}