{"id":29794,"date":"2020-04-23T16:26:59","date_gmt":"2020-04-23T16:26:59","guid":{"rendered":"https:\/\/www.iolife.eu\/wir-schaffen-gemeinsam\/advanced-genetic-testing\/"},"modified":"2020-12-11T12:43:51","modified_gmt":"2020-12-11T10:43:51","slug":"erweiterte-genetische-untersuchungen","status":"publish","type":"page","link":"https:\/\/www.iolife.eu\/de\/wir-schaffen-gemeinsam\/erweiterte-genetische-untersuchungen\/","title":{"rendered":"Erweiterte genetische Untersuchungen"},"content":{"rendered":"<div class=\"wpb-content-wrapper\" id=\"wpb-content-root\"><p>[vc_row full_height=&#8220;yes&#8220; type=&#8220;color&#8220; bg_color=&#8220;#000000&#8243; padding_top=&#8220;&#8220; padding_bottom=&#8220;&#8220;][vc_column]\n\t\t\t\t<p class=\"rs-p-wp-fix\"><\/p>\n\t\t\t\t<sr7-module data-alias=\"together-genetic-tests_en\" data-id=\"53\" id=\"SR7_53_1\" class=\"rs-ov-hidden\" data-version=\"6.8.1\">\n\t\t\t\t\t<sr7-adjuster><\/sr7-adjuster>\n\t\t\t\t\t<sr7-content>\n\t\t\t\t\t\t<sr7-slide id=\"SR7_53_1-92\" data-key=\"92\">\n\t\t\t\t\t\t\t<sr7-bg id=\"SR7_53_1-92-15\" class=\"sr7-layer\"><noscript><img decoding=\"async\" src=\"https:\/\/www.iolife.eu\/wp-content\/uploads\/2024\/05\/prohgmenoi-genetikoi-elegxoi.jpg\" alt=\"\" title=\"prohgmenoi-genetikoi-elegxoi\"><\/noscript><\/sr7-bg>\n\t\t\t\t\t\t\t<sr7-txt id=\"SR7_53_1-92-4\" class=\"sr7-layer\">Erweiterte genetische Untersuchungen <\/sr7-txt>\n\t\t\t\t\t\t\t<sr7-txt id=\"SR7_53_1-92-10\" class=\"sr7-layer\">Erweiterte genetische Untersuchungen tragen dazu bei, die \u00dcbertragung genetischer Krankheiten auf Kinder zu minimieren, aber auch eine bisher nicht nachweisbare Faktoren der Unfruchtbarkeit unbekannter Ursache zu behandeln. Gleichzeitig erlauben sie uns, nur die gesunden Embryonen, die w\u00e4hrend des IVF-Prozesses entstehen, in die Geb\u00e4rmutter zu \u00fcbertragen.<\/sr7-txt>\n\t\t\t\t\t\t\t<sr7-txt id=\"SR7_53_1-92-14\" class=\"sr7-layer\"><span><\/span><span><\/span><span><\/span><\/sr7-txt>\n\t\t\t\t\t\t<\/sr7-slide>\n\t\t\t\t\t\t<sr7-slide id=\"SR7_53_1-222\" data-key=\"222\">\n\t\t\t\t\t\t<\/sr7-slide>\n\t\t\t\t\t<\/sr7-content>\n\t\t\t\t\t<image_lists style=\"display:none\">\n\t\t\t\t\t\t<img data-src=\"\/\/www.iolife.eu\/wp-content\/uploads\/2024\/05\/prohgmenoi-genetikoi-elegxoi.jpg\" data-libid=\"35031\" data-lib=\"medialibrary\" title=\"prohgmenoi-genetikoi-elegxoi\" width=\"0\" height=\"0\" data-dbsrc=\"Ly93d3cuaW9saWZlLmV1L3dwLWNvbnRlbnQvdXBsb2Fkcy8yMDI0LzA1L3Byb2hnbWVub2ktZ2VuZXRpa29pLWVsZWd4b2kuanBn\"\/>\n\t\t\t\t\t<\/image_lists>\n\t\t\t\t<\/sr7-module>\n\t\t\t\t<script>\n\t\t\t\t\twindow.SR7 ??={};SR7.PMH ??={}; SR7.PMH[\"SR7_53_1\"] = {cn:100,state:false,fn: function() { if (window._tpt!==undefined && window._tpt.prepareModuleHeight !== undefined) {  _tpt.prepareModuleHeight({id:\"SR7_53_1\",el:[\"1080\",\"1080\",\"1024\",\"500\",\"400\"],type:'standard',shdw:'0',gh:[\"1080\",\"1080\",\"1024\",\"500\",\"400\"],gw:[\"1980\",\"1980\",\"1367\",\"778\",\"480\"],vpt:['-200px&#039;,&#039;-200px&#039;,&#039;-200px&#039;,&#039;-200px&#039;,&#039;-200px'],size:{fullWidth:true, fullHeight:true},fho:',',mh:'0',onh:0,onw:0,bg:{color:'{\"orig\":\"transparent\",\"type\":\"solid\",\"string\":\"transparent\"}'},plType:'-1',plColor:'#FFFFFF'});   SR7.PMH[\"SR7_53_1\"].state=true;} else if(SR7.PMH[\"SR7_53_1\"].cn-->0)\tsetTimeout( SR7.PMH[\"SR7_53_1\"].fn,19);}};SR7.PMH[\"SR7_53_1\" ].fn();\n\t\t\t\t<\/script>\n[\/vc_column][\/vc_row][vc_row equal_height=&#8220;yes&#8220; type=&#8220;color&#8220; bg_color=&#8220;#ededed&#8220; column_gap=&#8220;no&#8220; padding_top=&#8220;20&#8243; padding_bottom=&#8220;20&#8243;][vc_column width=&#8220;1\/3&#8243; css=&#8220;.vc_custom_1585566892921{margin-top: 20px !important;margin-right: 10px !important;margin-bottom: 20px !important;margin-left: 10px !important;border-top-width: 1px !important;border-right-width: 1px !important;border-bottom-width: 1px !important;border-left-width: 1px !important;background-color: #ffffff !important;border-left-color: #dbdbdb !important;border-left-style: solid !important;border-right-color: #dbdbdb !important;border-right-style: solid !important;border-top-color: #dbdbdb !important;border-top-style: solid !important;border-bottom-color: #dbdbdb !important;border-bottom-style: solid !important;}&#8220;][vc_single_image image=&#8220;15452&#8243; img_size=&#8220;500&#215;500&#8243; alignment=&#8220;center&#8220; full_width=&#8220;yes&#8220;][vc_custom_heading text=&#8220;PGT-A&#8220; font_container=&#8220;tag:h2|font_size:26|text_align:center|color:%23444444|line_height:1.2&#8243; use_theme_fonts=&#8220;yes&#8220; responsive_font=&#8220;yes&#8220; font_size_xs=&#8220;18&#8243; line_height_xs=&#8220;24&#8243; font_size_sm=&#8220;18&#8243; line_height_sm=&#8220;24&#8243; font_size_md=&#8220;22&#8243; line_height_md=&#8220;30&#8243; el_class=&#8220;iol-title&#8220;][vc_column_text animation=&#8220;animate-when-visible&#8220; css_animation=&#8220;el-fade&#8220; el_class=&#8220;iol-text&#8220; css=&#8220;.vc_custom_1607528306745{padding-right: 5% !important;padding-left: 5% !important;}&#8220;]Sie erm\u00f6glichen es uns, nur die Embryonen mit der richtigen Anzahl von Chromosomen auszuw\u00e4hlen, die sich einnisten und somit zur Geburt eines gesunden Kindes f\u00fchren.[\/vc_column_text]<style>#btn_6af59643c8570:hover {background-color: rgba(212,170,224,0.73) !important;color: #ffffff !important;border-color: rgba(193,193,193,0.01) !important;}<\/style><div class=\"text-center\"><a class=\"btn iol-button no-border-radius btn-custom\" href=\"https:\/\/www.iolife.eu\/de\/wir-schaffen-gemeinsam\/erweiterte-genetische-untersuchungen\/praeimplantations-gentests-von-chromosomen-pgt-a\/\" target=\"_blank\" style=\"background-color: #ffffff;color: #9e9e9e;border-color: #c1c1c1;\"id=\"btn_6af59643c8570\">Mehr erfahren<\/a><\/div>[\/vc_column][vc_column width=&#8220;1\/3&#8243; css=&#8220;.vc_custom_1585566885033{margin-top: 20px !important;margin-right: 10px !important;margin-bottom: 20px !important;margin-left: 10px !important;border-top-width: 1px !important;border-right-width: 1px !important;border-bottom-width: 1px !important;border-left-width: 1px !important;background-color: #ffffff !important;border-left-color: #dbdbdb !important;border-left-style: solid !important;border-right-color: #dbdbdb !important;border-right-style: solid !important;border-top-color: #dbdbdb !important;border-top-style: solid !important;border-bottom-color: #dbdbdb !important;border-bottom-style: solid !important;}&#8220;][vc_single_image image=&#8220;15453&#8243; img_size=&#8220;500&#215;500&#8243; alignment=&#8220;center&#8220; full_width=&#8220;yes&#8220;][vc_custom_heading text=&#8220;PGT-M&#8220; font_container=&#8220;tag:h2|font_size:26|text_align:center|color:%23444444|line_height:1.2&#8243; use_theme_fonts=&#8220;yes&#8220; responsive_font=&#8220;yes&#8220; font_size_xs=&#8220;18&#8243; line_height_xs=&#8220;24&#8243; font_size_sm=&#8220;18&#8243; line_height_sm=&#8220;24&#8243; font_size_md=&#8220;22&#8243; line_height_md=&#8220;30&#8243; el_class=&#8220;iol-title&#8220;][vc_column_text animation=&#8220;animate-when-visible&#8220; css_animation=&#8220;el-fade&#8220; el_class=&#8220;iol-text&#8220; css=&#8220;.vc_custom_1607528465582{padding-right: 5% !important;padding-left: 5% !important;}&#8220;]Um im Rahmen der medizinisch assistierten Reproduktion die Embryonen auszuw\u00e4hlen, die nicht die Krankheiten tragen, die von den Eltern herr\u00fchren, f\u00fchren wir die PGT-M.[\/vc_column_text]<style>#btn_6af59643c863d:hover {background-color: rgba(212,170,224,0.73) !important;color: #ffffff !important;border-color: rgba(193,193,193,0.01) !important;}<\/style><div class=\"text-center\"><a class=\"btn iol-button no-border-radius btn-custom\" href=\"https:\/\/www.iolife.eu\/de\/wir-schaffen-gemeinsam\/erweiterte-genetische-untersuchungen\/praeimplantations-gentests-fuer-monogene-krankheiten-pgt-m\/\" target=\"_blank\" style=\"background-color: #ffffff;color: #9e9e9e;border-color: #c1c1c1;\"id=\"btn_6af59643c863d\">Mehr erfahren<\/a><\/div>[\/vc_column][vc_column width=&#8220;1\/3&#8243; css=&#8220;.vc_custom_1585566860209{margin-top: 20px !important;margin-right: 10px !important;margin-bottom: 20px !important;margin-left: 10px !important;border-top-width: 1px !important;border-right-width: 1px !important;border-bottom-width: 1px !important;border-left-width: 1px !important;background-color: #ffffff !important;}&#8220;][vc_single_image image=&#8220;15451&#8243; img_size=&#8220;500&#215;500&#8243; alignment=&#8220;center&#8220; full_width=&#8220;yes&#8220;][vc_custom_heading text=&#8220;niPGT-A&#8220; font_container=&#8220;tag:h2|font_size:26|text_align:center|color:%23444444|line_height:1.2&#8243; use_theme_fonts=&#8220;yes&#8220; responsive_font=&#8220;yes&#8220; font_size_xs=&#8220;18&#8243; line_height_xs=&#8220;24&#8243; font_size_sm=&#8220;18&#8243; line_height_sm=&#8220;24&#8243; font_size_md=&#8220;22&#8243; line_height_md=&#8220;30&#8243; el_class=&#8220;iol-title&#8220;][vc_column_text animation=&#8220;animate-when-visible&#8220; css_animation=&#8220;el-fade&#8220; el_class=&#8220;iol-text&#8220; css=&#8220;.vc_custom_1607528495897{padding-right: 5% !important;padding-left: 5% !important;}&#8220;]Das bahnbrechende nicht-invasive Verfahren (niPGT) macht die Notwendigkeit einer fetalen Biopsie \u00fcberfl\u00fcssig und erleichtert den Zugang zur Kontrolle von Chromosomenanomalien bei F\u00f6ten aus allen IVF-Zyklen.[\/vc_column_text]<style>#btn_6af59643c86dc:hover {background-color: rgba(212,170,224,0.73) !important;color: #ffffff !important;border-color: rgba(193,193,193,0.01) !important;}<\/style><div class=\"text-center\"><a class=\"btn iol-button no-border-radius btn-custom\" href=\"https:\/\/www.iolife.eu\/de\/wir-schaffen-gemeinsam\/erweiterte-genetische-untersuchungen\/nicht-invasive-praeimplantations-gentests-von-chromosomen-nipgt-a\/\" target=\"_blank\" style=\"background-color: #ffffff;color: #9e9e9e;border-color: #c1c1c1;\"id=\"btn_6af59643c86dc\">Mehr erfahren<\/a><\/div>[\/vc_column][\/vc_row][vc_row equal_height=&#8220;yes&#8220; type=&#8220;color&#8220; bg_color=&#8220;#ededed&#8220; column_gap=&#8220;no&#8220; padding_top=&#8220;20&#8243; padding_bottom=&#8220;20&#8243;][vc_column width=&#8220;1\/3&#8243; css=&#8220;.vc_custom_1585566892921{margin-top: 20px !important;margin-right: 10px !important;margin-bottom: 20px !important;margin-left: 10px !important;border-top-width: 1px !important;border-right-width: 1px !important;border-bottom-width: 1px !important;border-left-width: 1px !important;background-color: #ffffff !important;border-left-color: #dbdbdb !important;border-left-style: solid !important;border-right-color: #dbdbdb !important;border-right-style: solid !important;border-top-color: #dbdbdb !important;border-top-style: solid !important;border-bottom-color: #dbdbdb !important;border-bottom-style: solid !important;}&#8220;][vc_single_image image=&#8220;25750&#8243; img_size=&#8220;500&#215;500&#8243; alignment=&#8220;center&#8220; full_width=&#8220;yes&#8220;][vc_custom_heading text=&#8220;Endometrialer Rezeptivit\u00e4tstest (ER Map, ERA-Test)&#8220; font_container=&#8220;tag:h2|font_size:26|text_align:center|color:%23444444|line_height:1.2&#8243; use_theme_fonts=&#8220;yes&#8220; responsive_font=&#8220;yes&#8220; font_size_xs=&#8220;18&#8243; line_height_xs=&#8220;24&#8243; font_size_sm=&#8220;18&#8243; 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width=&#8220;1\/3&#8243; css=&#8220;.vc_custom_1585566885033{margin-top: 20px !important;margin-right: 10px !important;margin-bottom: 20px !important;margin-left: 10px !important;border-top-width: 1px !important;border-right-width: 1px !important;border-bottom-width: 1px !important;border-left-width: 1px !important;background-color: #ffffff !important;border-left-color: #dbdbdb !important;border-left-style: solid !important;border-right-color: #dbdbdb !important;border-right-style: solid !important;border-top-color: #dbdbdb !important;border-top-style: solid !important;border-bottom-color: #dbdbdb !important;border-bottom-style: solid !important;}&#8220;][vc_single_image image=&#8220;28536&#8243; img_size=&#8220;500&#215;500&#8243; alignment=&#8220;center&#8220; full_width=&#8220;yes&#8220;][vc_custom_heading text=&#8220;Immunologische Analyse des Endometriums (IM Map)&#8220; font_container=&#8220;tag:h2|font_size:26|text_align:center|color:%23444444|line_height:1.2&#8243; use_theme_fonts=&#8220;yes&#8220; responsive_font=&#8220;yes&#8220; font_size_xs=&#8220;18&#8243; line_height_xs=&#8220;24&#8243; font_size_sm=&#8220;18&#8243; line_height_sm=&#8220;24&#8243; font_size_md=&#8220;22&#8243; line_height_md=&#8220;30&#8243; el_class=&#8220;iol-title&#8220;][vc_column_text animation=&#8220;animate-when-visible&#8220; css_animation=&#8220;el-fade&#8220; el_class=&#8220;iol-text&#8220; css=&#8220;.vc_custom_1607528647935{padding-right: 5% !important;padding-left: 5% !important;}&#8220;]Um eine erfolgreiche Schwangerschaft zu erreichen, ist es wichtig, dass die Stamm- und Embryonalzellen in einer Feinabstimmung des Immungleichgewichts koexistieren.[\/vc_column_text]<style>#btn_6af59643c88b9:hover {background-color: rgba(212,170,224,0.73) !important;color: #ffffff !important;border-color: rgba(193,193,193,0.01) !important;}<\/style><div class=\"text-center\"><a class=\"btn iol-button no-border-radius btn-custom\" href=\"https:\/\/www.iolife.eu\/de\/wir-schaffen-gemeinsam\/erweiterte-genetische-untersuchungen\/endometrial-immunological-testing-immap\/\" target=\"_blank\" style=\"background-color: #ffffff;color: #9e9e9e;border-color: #c1c1c1;\"id=\"btn_6af59643c88b9\">Mehr erfahren<\/a><\/div>[\/vc_column][vc_column width=&#8220;1\/3&#8243; css=&#8220;.vc_custom_1585566860209{margin-top: 20px !important;margin-right: 10px !important;margin-bottom: 20px !important;margin-left: 10px !important;border-top-width: 1px !important;border-right-width: 1px !important;border-bottom-width: 1px !important;border-left-width: 1px !important;background-color: #ffffff !important;}&#8220;][vc_single_image image=&#8220;25134&#8243; img_size=&#8220;500&#215;500&#8243; alignment=&#8220;center&#8220; full_width=&#8220;yes&#8220;][vc_custom_heading text=&#8220;KIR- und HLA-C Genotypisierung&#8220; font_container=&#8220;tag:h2|font_size:26|text_align:center|color:%23444444|line_height:1.2&#8243; use_theme_fonts=&#8220;yes&#8220; responsive_font=&#8220;yes&#8220; font_size_xs=&#8220;18&#8243; line_height_xs=&#8220;24&#8243; font_size_sm=&#8220;18&#8243; line_height_sm=&#8220;24&#8243; font_size_md=&#8220;22&#8243; line_height_md=&#8220;30&#8243; el_class=&#8220;iol-title&#8220;][vc_column_text animation=&#8220;animate-when-visible&#8220; css_animation=&#8220;el-fade&#8220; el_class=&#8220;iol-text&#8220; css=&#8220;.vc_custom_1607528718354{padding-right: 5% !important;padding-left: 5% !important;}&#8220;]Die Identifizierung von KIR und HLA-C ist ein genetischer Test, der es uns erlaubt, die Wahrscheinlichkeit einer Absto\u00dfung des F\u00f6tus (der F\u00f6ten) durch das Immunsystem der Mutter zu beurteilen.[\/vc_column_text]<style>#btn_6af59643c8982:hover {background-color: rgba(212,170,224,0.73) !important;color: #ffffff !important;border-color: rgba(193,193,193,0.01) !important;}<\/style><div class=\"text-center\"><a class=\"btn iol-button no-border-radius btn-custom\" href=\"https:\/\/www.iolife.eu\/de\/wir-schaffen-gemeinsam\/erweiterte-genetische-untersuchungen\/kir-und-hla-c-genotypisierung\/\" target=\"_blank\" style=\"background-color: #ffffff;color: #9e9e9e;border-color: #c1c1c1;\"id=\"btn_6af59643c8982\">Mehr erfahren<\/a><\/div>[\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row full_height=&#8220;yes&#8220; type=&#8220;color&#8220; bg_color=&#8220;#000000&#8243; padding_top=&#8220;&#8220; padding_bottom=&#8220;&#8220;][vc_column][\/vc_column][\/vc_row][vc_row equal_height=&#8220;yes&#8220; type=&#8220;color&#8220; bg_color=&#8220;#ededed&#8220; column_gap=&#8220;no&#8220; padding_top=&#8220;20&#8243; padding_bottom=&#8220;20&#8243;][vc_column width=&#8220;1\/3&#8243; css=&#8220;.vc_custom_1585566892921{margin-top: 20px !important;margin-right: 10px !important;margin-bottom: 20px !important;margin-left: 10px !important;border-top-width: 1px !important;border-right-width: 1px 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