{"id":33774,"date":"2022-11-26T11:07:54","date_gmt":"2022-11-26T11:07:54","guid":{"rendered":"https:\/\/gyncentrum.pl\/nosicielstwo-chorob-genetycznych\/"},"modified":"2024-05-22T20:43:00","modified_gmt":"2024-05-22T20:43:00","slug":"carrying-genetic-diseases","status":"publish","type":"servies","link":"https:\/\/gyncentrum.pl\/en\/carrying-genetic-diseases\/","title":{"rendered":"Carrying genetic diseases"},"content":{"rendered":"\n    <section id=\"spacer-block_8cff1e16cad0d715200a824ae34929fe\"\n             class=\"block-spacer  height-32px background-transparent\">\n    <\/section>\n\n<div class=\"container\">\n<h1 class=\"wp-block-heading\">Nosicielstwo chor\u00f3b genetycznych <\/h1>\n<\/div>\n    <section id=\"spacer-block_8cff1e16cad0d715200a824ae34929fe\"\n             class=\"block-spacer  height-32px background-transparent\">\n    <\/section>\n\n\n<section id=\"services-list-block_503918523c3a1a3696d5ff58074e068c\" class=\"block-services-list \">\n    <div class=\"container\">\n        <div class=\"top-part\">\n                                            <\/div>\n        <div class=\"grid-part\">\n                                                    <a class=\"single-service\" href=\"https:\/\/gyncentrum.pl\/en\/carrying-genetic-diseases\/thrombophilia-congenital-hypercoagulability\/\">\n                    <div class=\"service-title title--h5\">Thrombophilia &#8211; congenital hypercoagulability<\/div>\n                    <div class=\"service-excerpt\"><p>Congenital thrombophilia &#8211; hypercoagulability, is a genetically determined tendency to develop blood clots. It is one of the main risk factors for venous thromboembolism.<\/p>\n<\/div>\n                    <div class=\"fz-button  new-button-style new-color-style-orange-100 new-fill-style-border\">\n                        <span class=\"text-itself\">Czytaj wi\u0119cej <\/span>\n                        <svg width=\"22\" height=\"14\" viewBox=\"0 0 22 14\" fill=\"none\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"><path fill-rule=\"evenodd\" clip-rule=\"evenodd\" d=\"M0.5 7C0.5 6.58579 0.835786 6.25 1.25 6.25L18.9393 6.25L14.2197 1.53033C13.9268 1.23744 13.9268 0.762562 14.2197 0.469669C14.5126 0.176776 14.9874 0.176776 15.2803 0.469669L21.2803 6.46967C21.5732 6.76256 21.5732 7.23744 21.2803 7.53033L15.2803 13.5303C14.9874 13.8232 14.5126 13.8232 14.2197 13.5303C13.9268 13.2374 13.9268 12.7626 14.2197 12.4697L18.9393 7.75L1.25 7.75C0.835786 7.75 0.5 7.41421 0.5 7Z\" fill=\"#ffffff\"><\/path><\/svg>\n                    <\/div>\n                <\/a>\n                                <a class=\"single-service\" href=\"https:\/\/gyncentrum.pl\/en\/carrying-genetic-diseases\/frax-fragile-x-chromosome-syndrome\/\">\n                    <div class=\"service-title title--h5\">FRAX &#8211; fragile X chromosome syndrome<\/div>\n                    <div class=\"service-excerpt\"><p>Fragile X syndrome (FRAX) is associated with the occurrence of a dynamic mutation in the FMR1 gene, which results in inhibition of its expression and consequent lack of FMRP protein synthesis. <\/p>\n<\/div>\n                    <div class=\"fz-button  new-button-style new-color-style-orange-100 new-fill-style-border\">\n                        <span class=\"text-itself\">Czytaj wi\u0119cej <\/span>\n                        <svg width=\"22\" height=\"14\" viewBox=\"0 0 22 14\" fill=\"none\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"><path fill-rule=\"evenodd\" clip-rule=\"evenodd\" d=\"M0.5 7C0.5 6.58579 0.835786 6.25 1.25 6.25L18.9393 6.25L14.2197 1.53033C13.9268 1.23744 13.9268 0.762562 14.2197 0.469669C14.5126 0.176776 14.9874 0.176776 15.2803 0.469669L21.2803 6.46967C21.5732 6.76256 21.5732 7.23744 21.2803 7.53033L15.2803 13.5303C14.9874 13.8232 14.5126 13.8232 14.2197 13.5303C13.9268 13.2374 13.9268 12.7626 14.2197 12.4697L18.9393 7.75L1.25 7.75C0.835786 7.75 0.5 7.41421 0.5 7Z\" fill=\"#ffffff\"><\/path><\/svg>\n                    <\/div>\n                <\/a>\n                                    <\/div>\n    <\/div>\n<\/section>\n","protected":false},"excerpt":{"rendered":"<p>Nosicielstwo chor\u00f3b genetycznych<\/p>\n","protected":false},"featured_media":8579,"parent":0,"menu_order":372,"template":"","class_list":["post-33774","servies","type-servies","status-publish","has-post-thumbnail","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/gyncentrum.pl\/en\/wp-json\/wp\/v2\/servies\/33774","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/gyncentrum.pl\/en\/wp-json\/wp\/v2\/servies"}],"about":[{"href":"https:\/\/gyncentrum.pl\/en\/wp-json\/wp\/v2\/types\/servies"}],"version-history":[{"count":3,"href":"https:\/\/gyncentrum.pl\/en\/wp-json\/wp\/v2\/servies\/33774\/revisions"}],"predecessor-version":[{"id":40460,"href":"https:\/\/gyncentrum.pl\/en\/wp-json\/wp\/v2\/servies\/33774\/revisions\/40460"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/gyncentrum.pl\/en\/wp-json\/wp\/v2\/media\/8579"}],"wp:attachment":[{"href":"https:\/\/gyncentrum.pl\/en\/wp-json\/wp\/v2\/media?parent=33774"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}