js_composer
domain was triggered too early. This is usually an indicator for some code in the plugin or theme running too early. Translations should be loaded at the init
action or later. Please see Debugging in WordPress for more information. (This message was added in version 6.7.0.) in /home4/ccexzmte/geneticcounselor.ae/wp-includes/functions.php on line 6121psychologycare
domain was triggered too early. This is usually an indicator for some code in the plugin or theme running too early. Translations should be loaded at the init
action or later. Please see Debugging in WordPress for more information. (This message was added in version 6.7.0.) in /home4/ccexzmte/geneticcounselor.ae/wp-includes/functions.php on line 6121Inherited vs Non-inherited Cancer We all carry certain genes (instruction codes) that are normally protective against cancer\u00a0\u2013 they correct any DNA damage that naturally occurs when cells divide.<\/p>\n Inheriting\u00a0faulty versions or “variants” of these genes \u2013 mutations, significantly raises your risk of developing cancer because the altered genes cannot repair the damaged cells which can build up and form a tumor (cancer).<\/p>\n Cancer is not usually inherited (in the family), but<\/strong>\u00a0<\/strong>some types\u00a0\u2013 mainly breast, ovarian, colorectal\u00a0and prostate cancer\u00a0\u2013 can be strongly influenced by genes and can<\/strong>\u00a0<\/strong>run in families<\/strong>. Of diagnosed breast cancer cases, only 5-10% are hereditary<\/strong>; meaning they occur due to an inherited <\/strong>genetic change in the family.<\/p>\n Panel Testing WHO SHOULD HAVE A GENETIC TEST? <\/strong><\/p>\n Advantages of testing:<\/strong><\/p>\n Disadvantages to testing for BRCA mutations:<\/strong><\/p>\n What sort of results to expect?<\/strong><\/p>\n Positive Result:<\/strong> A cancer-causing mutation is identified – risk for associated cancers is increased.<\/p>\n First-degree relatives, including parents, siblings, and children, have a 50% chance to carry the same mutation.<\/p>\n Genetic counseling is recommended for all family members to clarify their risks.<\/p>\n Negative Result:<\/strong> No breast cancer-causing mutation is detected in the genes included in the panel.<\/p>\n The significance of a negative result is dependent upon each individual\u2019s personal family history. It is important to discuss the<\/p>\n significance of a negative result with your physician or genetic counselor.<\/p>\n Variant of Unclassified Significance:<\/strong> A genetic change referred to as a variant is identified in one of the genes in the cancer panel.<\/p>\n Variants, which are changes in the gene structure, may or may not have a harmful effect on how the gene functions.<\/p>\n The laboratory does not have enough information to determine if the variant results in an increased risk for cancer or not. Further research needs to be carried out to understand whether the change is harmful or not.<\/p>\n Should people considering genetic testing talk with a genetic counselor?<\/strong><\/p>\n Genetic counseling is generally recommended before and after any genetic test for an inherited cancer syndrome. This counseling should be performed by a health care professional who is experienced in cancer genetics and counseling. Genetic counseling usually covers many aspects of the testing process, including:<\/p>\n Inherited vs Non-inherited Cancer Breast cancer is the most common female cancer affecting approximately 1 out of 8 women (~12%). The majority of breast cancer cases occur by chance, also referred to as sporadic. We all carry certain genes (instruction codes) that are normally protective against cancer\u00a0\u2013 they correct any DNA damage that naturally occurs<\/p>\n","protected":false},"author":1,"featured_media":1457,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[294],"tags":[253,254,255,256],"class_list":["post-1455","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blogs-articles","tag-breast-cancer","tag-hereditary-breast-cancer","tag-significance-of-a-negative-result","tag-testing-for-breast-cancer"],"_links":{"self":[{"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/posts\/1455","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/comments?post=1455"}],"version-history":[{"count":7,"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/posts\/1455\/revisions"}],"predecessor-version":[{"id":1465,"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/posts\/1455\/revisions\/1465"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/media\/1457"}],"wp:attachment":[{"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/media?parent=1455"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/categories?post=1455"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.geneticcounselor.ae\/wp-json\/wp\/v2\/tags?post=1455"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
\n<\/strong>Breast cancer is the most common female cancer affecting approximately 1 out of 8 women (~12%). The majority of breast cancer cases occur by chance, also referred to as sporadic.<\/p>\n
\n<\/strong>Multiple genes responsible for hereditary breast cancer have been discovered. Approximately 25% of hereditary breast cancer is due to mutations in one of two genes called BRCA1 and BRCA2. Another 20% of hereditary breast cancer is due to other known hereditary cancer genes. The application of \u2018panel testing\u2019 for breast cancer genetic testing is so far a matter of discussion. Standard practice still follows; in a first step, carrying out a BRCA 1 and 2 genetic test to identify any breast cancer causing mutations. However, if the woman tests negative, in a second step, she could then be offered a panel test of 21 (or more) breast cancer related genes to identify the disease causing mutation.<\/p>\n\n
\n
\n
\n
\n