{"id":7549,"date":"2021-02-23T14:42:35","date_gmt":"2021-02-23T11:42:35","guid":{"rendered":"https:\/\/locus-medicus.gr\/xrwmoswmikos-elegxos-karyotypos\/"},"modified":"2022-08-01T14:50:29","modified_gmt":"2022-08-01T11:50:29","slug":"xrwmoswmikos-elegxos-karyotypos","status":"publish","type":"page","link":"https:\/\/locus-medicus.gr\/en\/eidikes-eksetaseis-gynaika\/xrwmoswmikos-elegxos-karyotypos\/","title":{"rendered":"Chromosomal Testing (Karyotype)"},"content":{"rendered":"<p>[vc_row full_width=&#8221;stretch_row&#8221; background_color=&#8221;custom&#8221; custom_background_color=&#8221;#222222&#8243;][vc_column]\n\t\t\t<!-- START xrwmoswmikoselegxoskaryotypos REVOLUTION SLIDER 6.3.3 --><p class=\"rs-p-wp-fix\"><\/p>\n\t\t\t<rs-module-wrap id=\"rev_slider_45_1_wrapper\" data-source=\"gallery\" style=\"background:transparent;padding:0;margin:0px auto;margin-top:0;margin-bottom:0;\">\n\t\t\t\t<rs-module id=\"rev_slider_45_1\" style=\"\" 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-->\n[\/vc_column][\/vc_row][vc_row lg_spacing=&#8221;padding_top:145;padding_bottom:145&#8243; sm_spacing=&#8221;padding_top:100;padding_bottom:100&#8243;][vc_column offset=&#8221;vc_col-md-4&#8243;][tm_heading custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Karyotypic fetal abnormalities exceed 50% of spontaneous first trimester miscarriages.&#8221; font_size=&#8221;sm:24;md:30;lg:36&#8243; line_height=&#8221;1.42&#8243;][tm_spacer size=&#8221;sm:40&#8243;][\/vc_column][vc_column offset=&#8221;vc_col-md-offset-1 vc_col-md-7&#8243;][tm_heading custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Chromosomal Testing (Karyotype)&#8221; font_size=&#8221;lg:18&#8243; line_height=&#8221;1.39&#8243;][tm_spacer size=&#8221;lg:20&#8243;][tm_heading tag=&#8221;div&#8221; custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Chromosomal Testing of Woman and Fetus&#8221; font_size=&#8221;lg:18&#8243; line_height=&#8221;1.62&#8243;][tm_spacer size=&#8221;lg:30&#8243;][tm_heading tag=&#8221;div&#8221; custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Chromosomal testing, i.e. karyotype, is provided in cases of regressions as well as infertility.&#8221;][\/vc_column][\/vc_row][vc_row][vc_column width=&#8221;1\/2&#8243;][vc_column_text]<\/p>\n<p class=\"p1\">It is reported that karyotypic abnormalities of the fetus exceed 50% of the first trimester spontaneous miscarriages. However, most of the times no diagnostic abrasion is performed and thus no material is obtained for examination of Karyotypic Analysis of miscarriages Products. When serial miscarriages have happened, it is important to be determined if the cause concerns karyotype abnormalities or not. Usually in cases with abnormal embryos nature acts properly, rejecting the embryos and effectively protecting the population from abnormal organisms by birth. These pregnancies cannot be saved. They usually affect older women and there is no way to prevent them from recurring.<\/p>\n<p class=\"p1\">The karyotypic abnormalities with chromosomal permutations or other related lesions of the prospective parents are an important part of the couple&#8217;s investigation into both a history of infertility and spontaneous miscarriages. Usually in these couples the pre\u2013implantation of the embryos with a process of assisted reproduction is recommended, in order to exclude abnormal embryos.<\/p>\n<p>[\/vc_column_text][tm_spacer size=&#8221;lg:50&#8243;][\/vc_column][vc_column width=&#8221;1\/2&#8243;][tm_image image_size=&#8221;custom&#8221; align=&#8221;right&#8221; sm_align=&#8221;center&#8221; image=&#8221;6365&#8243; image_size_width=&#8221;745&#8243; image_size_height=&#8221;680&#8243;][tm_spacer size=&#8221;sm:50&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][tm_spacer size=&#8221;lg:50&#8243;][vc_column_text]<\/p>\n<p class=\"p1\"><b>Woman \/ Couple Chromosomal Test<\/b><\/p>\n<ul>\n<li>\n<p class=\"p1\">Woman&#8217;s peripheral blood karyotype<\/p>\n<\/li>\n<li>\n<p class=\"p1\">Couple&#8217;s peripheral blood karyotype<\/p>\n<\/li>\n<\/ul>\n<p class=\"p1\"><b>Fetal Chromosomal \/ Genetic Testing<\/b><\/p>\n<div>\n<ul>\n<li>\n<p class=\"p1\">Amniotic fluid \/ chorionic villi karyotype<\/p>\n<\/li>\n<li>\n<p class=\"p1\">Amniotic fluid \/ chorionic villi karyotype, QF\u2013PCR, detection of delF508 mutation<\/p>\n<\/li>\n<li>\n<p class=\"p1\">Amniotic fluid \/ chorionic villus sampling karyotype, QF\u2013PCR, detection of delF508 and MLPA 21 mutation (detection of 21 micro\u2013deficiencies or micro-duplications)<\/p>\n<\/li>\n<li>\n<p class=\"p1\">NIPT \u2013 Non\u2013invasive prenatal testing from the mother&#8217;s blood<\/p>\n<\/li>\n<\/ul>\n<\/div>\n<div class=\"article-footer-wrap\">\n<div class=\"article-footer-top\">\n<div class=\"helix-social-share\">\n<div class=\"helix-social-share-icon\"><\/div>\n<\/div>\n<\/div>\n<\/div>\n<p>[\/vc_column_text][tm_spacer size=&#8221;lg:50&#8243;][\/vc_column][\/vc_row][vc_row full_width=&#8221;stretch_row&#8221; content_placement=&#8221;middle&#8221; background_color=&#8221;primary&#8221; lg_spacing=&#8221;padding_top:69;padding_bottom:69&#8243;][vc_column width=&#8221;1\/2&#8243;][tm_heading custom_google_font=&#8221;&#8221; xs_align=&#8221;center&#8221; text_color=&#8221;custom&#8221; custom_text_color=&#8221;#ffffff&#8221; text=&#8221;Book your appointment today&#8221;][tm_spacer size=&#8221;xs:30&#8243;][\/vc_column][vc_column width=&#8221;1\/2&#8243;][tm_button button=&#8221;url:tel%3A00302106544444|title:%2B30-210%2065%2044%20444&#8243; align=&#8221;right&#8221; xs_align=&#8221;center&#8221; color=&#8221;custom&#8221; button_bg_color=&#8221;custom&#8221; font_color=&#8221;primary&#8221; button_border_color=&#8221;custom&#8221; custom_button_bg_color=&#8221;#ffffff&#8221; custom_button_border_color=&#8221;#ffffff&#8221;][\/vc_column][\/vc_row]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>[vc_row full_width=&#8221;stretch_row&#8221; background_color=&#8221;custom&#8221; custom_background_color=&#8221;#222222&#8243;][vc_column][\/vc_column][\/vc_row][vc_row lg_spacing=&#8221;padding_top:145;padding_bottom:145&#8243; sm_spacing=&#8221;padding_top:100;padding_bottom:100&#8243;][vc_column offset=&#8221;vc_col-md-4&#8243;][tm_heading custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Karyotypic fetal abnormalities exceed 50% of spontaneous first trimester miscarriages.&#8221; font_size=&#8221;sm:24;md:30;lg:36&#8243; line_height=&#8221;1.42&#8243;][tm_spacer size=&#8221;sm:40&#8243;][\/vc_column][vc_column offset=&#8221;vc_col-md-offset-1 vc_col-md-7&#8243;][tm_heading custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Chromosomal Testing (Karyotype)&#8221; font_size=&#8221;lg:18&#8243; line_height=&#8221;1.39&#8243;][tm_spacer size=&#8221;lg:20&#8243;][tm_heading tag=&#8221;div&#8221; custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Chromosomal Testing of Woman and Fetus&#8221; font_size=&#8221;lg:18&#8243; line_height=&#8221;1.62&#8243;][tm_spacer size=&#8221;lg:30&#8243;][tm_heading tag=&#8221;div&#8221; custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Chromosomal testing, i.e. karyotype, is provided in cases of regressions as well as infertility.&#8221;][\/vc_column][\/vc_row][vc_row][vc_column width=&#8221;1\/2&#8243;][vc_column_text] It is reported that karyotypic abnormalities of the fetus exceed 50% of the first trimester spontaneous miscarriages. However, most of the times no diagnostic abrasion is performed and thus no material is obtained for examination of Karyotypic Analysis of miscarriages Products. When serial miscarriages have happened, it is important to be determined if the cause concerns karyotype abnormalities or not. Usually in cases with abnormal embryos nature acts properly, rejecting the embryos and effectively protecting the population from abnormal organisms by birth. These pregnancies cannot be saved. They usually affect older women and there is no way to prevent them from recurring. The karyotypic abnormalities with chromosomal permutations or other related lesions of the prospective parents are an important part of the couple&#8217;s investigation into both a history of infertility and spontaneous miscarriages. Usually in these couples the pre\u2013implantation of the embryos with a process of assisted reproduction is recommended, in order to exclude abnormal embryos. [\/vc_column_text][tm_spacer size=&#8221;lg:50&#8243;][\/vc_column][vc_column width=&#8221;1\/2&#8243;][tm_image image_size=&#8221;custom&#8221; align=&#8221;right&#8221; sm_align=&#8221;center&#8221; image=&#8221;6365&#8243; image_size_width=&#8221;745&#8243; image_size_height=&#8221;680&#8243;][tm_spacer size=&#8221;sm:50&#8243;][\/vc_column][\/vc_row][vc_row][vc_column][tm_spacer size=&#8221;lg:50&#8243;][vc_column_text] Woman \/ Couple Chromosomal Test Woman&#8217;s peripheral blood karyotype Couple&#8217;s peripheral blood karyotype Fetal Chromosomal \/ Genetic Testing Amniotic fluid \/ chorionic villi karyotype Amniotic fluid \/ chorionic villi karyotype, QF\u2013PCR, detection of delF508 mutation Amniotic fluid \/ chorionic villus sampling karyotype, QF\u2013PCR, detection of delF508 and MLPA 21 mutation (detection of 21 micro\u2013deficiencies or micro-duplications) NIPT \u2013 Non\u2013invasive prenatal testing from the mother&#8217;s blood [\/vc_column_text][tm_spacer size=&#8221;lg:50&#8243;][\/vc_column][\/vc_row][vc_row full_width=&#8221;stretch_row&#8221; 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background_color=&#8221;custom&#8221; custom_background_color=&#8221;#222222&#8243;][vc_column][\/vc_column][\/vc_row][vc_row lg_spacing=&#8221;padding_top:145;padding_bottom:145&#8243; sm_spacing=&#8221;padding_top:100;padding_bottom:100&#8243;][vc_column offset=&#8221;vc_col-md-4&#8243;][tm_heading custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Karyotypic fetal abnormalities exceed 50% of spontaneous first trimester miscarriages.&#8221; font_size=&#8221;sm:24;md:30;lg:36&#8243; line_height=&#8221;1.42&#8243;][tm_spacer size=&#8221;sm:40&#8243;][\/vc_column][vc_column offset=&#8221;vc_col-md-offset-1 vc_col-md-7&#8243;][tm_heading custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Chromosomal Testing (Karyotype)&#8221; font_size=&#8221;lg:18&#8243; line_height=&#8221;1.39&#8243;][tm_spacer size=&#8221;lg:20&#8243;][tm_heading tag=&#8221;div&#8221; custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Chromosomal Testing of Woman and Fetus&#8221; font_size=&#8221;lg:18&#8243; line_height=&#8221;1.62&#8243;][tm_spacer size=&#8221;lg:30&#8243;][tm_heading tag=&#8221;div&#8221; custom_google_font=&#8221;&#8221; google_fonts=&#8221;font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:300%20light%20regular%3A300%3Anormal&#8221; text=&#8221;Chromosomal testing, i.e. karyotype, is provided in cases of regressions as well as infertility.&#8221;][\/vc_column][\/vc_row][vc_row][vc_column width=&#8221;1\/2&#8243;][vc_column_text] It is reported that karyotypic abnormalities of the fetus exceed 50% of the first trimester spontaneous miscarriages. However, most of the times no diagnostic abrasion is performed and thus no material is obtained for examination of Karyotypic Analysis of miscarriages Products. When serial miscarriages have happened, it is important to be determined if the cause concerns karyotype abnormalities or not. Usually in cases with abnormal embryos nature acts properly, rejecting the embryos and effectively protecting the population from abnormal organisms by birth. These pregnancies cannot be saved. They usually affect older women and there is no way to prevent them from recurring. The karyotypic abnormalities with chromosomal permutations or other related lesions of the prospective parents are an important part of the couple&#8217;s investigation into both a history of infertility and spontaneous miscarriages. Usually in these couples the pre\u2013implantation of the embryos with a process of assisted reproduction is recommended, in order to exclude abnormal embryos. 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