{"id":42179,"date":"2018-02-26T11:06:38","date_gmt":"2018-02-26T11:06:38","guid":{"rendered":"https:\/\/sistemasgenomicos.digitis.net\/specialists\/precision-diagnosis\/prenatal-stage\/prenatal-genetic-diagnosis\/"},"modified":"2023-04-17T18:17:47","modified_gmt":"2023-04-17T16:17:47","slug":"prenatal-genetic-diagnosis","status":"publish","type":"page","link":"https:\/\/sistemasgenomicos.com\/en\/specialists\/precision-diagnosis\/prenatal-stage\/prenatal-genetic-diagnosis\/","title":{"rendered":"Prenatal Genetic Diagnosis"},"content":{"rendered":"\n  <div class=\"banner has-hover\" id=\"banner-2139834518\">\n          <div class=\"banner-inner fill\">\n        <div class=\"banner-bg fill\" >\n            <div class=\"bg fill bg-fill \"><\/div>\n                        <div class=\"overlay\"><\/div>            \n                    <\/div>\n\t\t\n        <div class=\"banner-layers container\">\n            <div class=\"fill banner-link\"><\/div>            \n   <div id=\"text-box-1533036442\" class=\"text-box banner-layer x50 md-x50 lg-x50 y50 md-y50 lg-y50 res-text\">\n                                <div class=\"text-box-content text dark text-shadow-2\">\n              \n              <div class=\"text-inner text-center\">\n                  \n<h1><span style=\"font-size: 85%;\">PRENATAL GENETIC DIAGNOSIS<\/span><\/h1>\n<h4><\/h4>\n<a href=\"https:\/\/clientes.sistemasgenomicos.com\/sglab\/en\/site\/login.html\" target=\"blank\" class=\"button primary is-small\"  >\n    <span>Request Service<\/span>\n  <i class=\"icon-angle-right\" aria-hidden=\"true\" ><\/i><\/a>\n\n<a href=\"https:\/\/sistemasgenomicos.com\/en\/about-us\/contact\/\" class=\"button white is-outline is-small\"  >\n    <span>Request Information<\/span>\n  <\/a>\n <a href=\"https:\/\/sistemasgenomicos.com\/en\/specialists\/biomedicine-services\/\" class=\"button white is-outline is-small\"  style=\"border-radius:99px;\">\n    <span>Check Catalog<\/span>\n  <\/a>\n\r\n\n              <\/div>\n           <\/div>\n                            \n<style>\n#text-box-1533036442 {\n  width: 81%;\n}\n#text-box-1533036442 .text-box-content {\n  font-size: 100%;\n}\n<\/style>\n    <\/div>\n \n        <\/div>\n      <\/div>\n\n            \n<style>\n#banner-2139834518 {\n  padding-top: 300px;\n}\n#banner-2139834518 .bg.bg-loaded {\n  background-image: url(https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/laboratorio-citogenetica4.jpg);\n}\n#banner-2139834518 .overlay {\n  background-color: rgba(6, 6, 6, 0.32);\n}\n#banner-2139834518 .bg {\n  background-position: 63% 66%;\n}\n<\/style>\n  <\/div>\n\n\n  <div id=\"page-header-891844669\" class=\"page-header-wrapper\">\n  <div class=\"page-title light simple-title\">\n\n    \n    <div class=\"page-title-inner container align-top flex-row medium-flex-wrap row-reverse\" >\n            <div class=\"title-content flex-col flex-left text-left medium-text-center\">\n        <div class=\"title-breadcrumbs pb-half pt-half\"><nav class=\"woocommerce-breadcrumb breadcrumbs uppercase\">Home<\/nav><\/div>      <\/div>\n    <\/div>\n\n     \n<style>\n#page-header-891844669 {\n  margin-bottom: 0px;\n}\n<\/style>\n  <\/div>\n    <\/div>\n  \n\t<div id=\"gap-1925318843\" class=\"gap-element clearfix\" style=\"display:block; height:auto;\">\n\t\t\n<style>\n#gap-1925318843 {\n  padding-top: 30px;\n}\n<\/style>\n\t<\/div>\n\t\n<div class=\"row\"  id=\"row-1956017723\">\n\n\t<div id=\"col-1941960446\" class=\"col medium-3 small-12 large-3\"  >\n\t\t\t\t<div class=\"col-inner\" style=\"background-color:rgb(249, 249, 249);\" >\n\t\t\t\n\t\t\t\n<div class=\"container section-title-container\" style=\"margin-bottom:0px;\"><h3 class=\"section-title section-title-normal\"><b><\/b><span class=\"section-title-main\" style=\"font-size:75%;\">PRENATAL Stage<\/span><b><\/b><\/h3><\/div>\n<div class=\"nav-wrapper\"><ul class=\"nav nav-uppercase nav-vertical nav-simple text-left nav-left\"><p class=\"lead shortcode-error text-center\">Sorry, no pages was found<\/p><\/ul><\/div>\n\t\t<\/div>\n\t\t\t\t\n<style>\n#col-1941960446 > .col-inner {\n  padding: 10px 10px 10px 10px;\n}\n<\/style>\n\t<\/div>\n\n\t\n\n\t<div id=\"col-30803523\" class=\"col medium-9 small-12 large-9\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<div class=\"row row-dashed\"  id=\"row-1579126163\">\n\n\t<div id=\"col-1329439070\" class=\"col medium-6 small-12 large-6\"  >\n\t\t\t\t<div class=\"col-inner text-left\"  >\n\t\t\t\n\t\t\t\n<h2 style=\"text-align: left;\">Prenatal Genetic Diagnosis<\/h2>\n<p><span style=\"font-size: 90%;\">Roughly 15% of the world\u2019s population (estimations from 2010) has learning disabilities and 1 in every 33 new-borns has congenital anomalies. These disorders have severe effects and generally involve a deterioration of cognitive and adaptive abilities. <\/span><\/p>\n<p><span style=\"font-size: 90%;\">It is estimated that the main etiological cause of these disorders is genetic factors.<\/span><\/p>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n\n\t<div id=\"col-675784600\" class=\"col medium-6 small-12 large-6\"  >\n\t\t\t\t<div class=\"col-inner text-left\"  >\n\t\t\t\n\t\t\t\n<p><span style=\"font-size: 90%;\">The prevalence of learning disabilities along with congenital anomalies make up for about 14% of all births.<\/span><span style=\"font-size: 90%;\">It is estimated that 3-6% of new-borns have some kind of congenital anomaly, in many cases with a genetic cause; the most common risk factors are family background, advanced age of the mother or having previously had a child with a chromosome syndrome. <\/span><\/p>\n<p><span style=\"font-size: 90%;\">Affected individuals have a huge challenge to survive including pathologies in various organs and physical limitations, and those associated with mobility, learning and social interaction. <\/span><\/p>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n<\/div>\n<div class=\"container section-title-container\" ><h3 class=\"section-title section-title-center\"><b><\/b><span class=\"section-title-main\" >Services<\/span><b><\/b><\/h3><\/div>\n\t<div id=\"gap-1789811969\" class=\"gap-element clearfix\" style=\"display:block; height:auto;\">\n\t\t\n<style>\n#gap-1789811969 {\n  padding-top: 30px;\n}\n<\/style>\n\t<\/div>\n\t\n\t<section class=\"section has-mask mask-arrow\" id=\"section_1850937780\">\n\t\t<div class=\"bg section-bg fill bg-fill  bg-loaded\" >\n\n\t\t\t\n\t\t\t\n\t\t\t\n\n\t\t<\/div>\n\n\t\t\n\n\t\t<div class=\"section-content relative\">\n\t\t\t\n<div class=\"row\"  id=\"row-1635982727\">\n\n\t<div id=\"col-148155616\" class=\"col medium-3 small-12 large-3\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n\t<div class=\"img has-hover x md-x lg-x y md-y lg-y\" id=\"image_1878578607\">\n\t\t\t\t\t\t\t\t<div class=\"img-inner image-cover dark\" style=\"padding-top:180px;\">\n\t\t\t<img loading=\"lazy\" decoding=\"async\" width=\"1020\" height=\"679\" src=\"https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/precision_hero-1024x682.jpg\" class=\"attachment-large size-large\" alt=\"\" srcset=\"https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/precision_hero-1024x682.jpg 1024w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/precision_hero-300x200.jpg 300w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/precision_hero-768x512.jpg 768w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/precision_hero-209x139.jpg 209w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/precision_hero-418x279.jpg 418w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/precision_hero-837x558.jpg 837w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/precision_hero.jpg 2000w\" sizes=\"auto, (max-width: 1020px) 100vw, 1020px\" \/>\t\t\t\t\t\t\n\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\n<style>\n#image_1878578607 {\n  width: 100%;\n}\n<\/style>\n\t<\/div>\n\t\n<a href=\"https:\/\/clientes.sistemasgenomicos.com\/sglab\/en\/site\/login.html\" target=\"blank\" class=\"button primary is-small\"  >\n    <span>Request Service<\/span>\n  <i class=\"icon-angle-right\" aria-hidden=\"true\" ><\/i><\/a>\n\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n\n\t<div id=\"col-1775331520\" class=\"col medium-9 small-12 large-9\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<h2 style=\"text-align: left;\">Conventional and Molecular Cytogenetics<\/h2>\n<p>The conventional cytogenetic study, carrying out a karyotype, allows us to study numerical and\/or structural abnormalities (insertions, translocations, deletions, duplications, etc.), with reference to any chromosome with an estimated resolution of 7-8 Mb.<\/p>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n<\/div>\n\t\t<\/div>\n\n\t\t\n<style>\n#section_1850937780 {\n  padding-top: 50px;\n  padding-bottom: 50px;\n  background-color: rgba(54, 97, 159, 0.05);\n}\n<\/style>\n\t<\/section>\n\t\n\t<section class=\"section has-mask mask-arrow\" id=\"section_795720642\">\n\t\t<div class=\"bg section-bg fill bg-fill  bg-loaded\" >\n\n\t\t\t\n\t\t\t\n\t\t\t\n\n\t\t<\/div>\n\n\t\t\n\n\t\t<div class=\"section-content relative\">\n\t\t\t\n<div class=\"row\"  id=\"row-772036949\">\n\n\t<div id=\"col-494810386\" class=\"col medium-3 small-12 large-3\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n\t<div class=\"img has-hover x md-x lg-x y md-y lg-y\" id=\"image_509858668\">\n\t\t\t\t\t\t\t\t<div class=\"img-inner image-cover dark\" style=\"padding-top:180px;\">\n\t\t\t<img loading=\"lazy\" decoding=\"async\" width=\"1000\" height=\"666\" src=\"https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/arrays1.jpg\" class=\"attachment-large size-large\" alt=\"\" srcset=\"https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/arrays1.jpg 1000w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/arrays1-300x200.jpg 300w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/arrays1-768x511.jpg 768w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/arrays1-209x139.jpg 209w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/arrays1-418x278.jpg 418w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/arrays1-837x557.jpg 837w\" sizes=\"auto, (max-width: 1000px) 100vw, 1000px\" \/>\t\t\t\t\t\t\n\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\n<style>\n#image_509858668 {\n  width: 100%;\n}\n<\/style>\n\t<\/div>\n\t\n<a href=\"https:\/\/clientes.sistemasgenomicos.com\/sglab\/en\/site\/login.html\" target=\"blank\" class=\"button primary is-small\"  >\n    <span>Request Service<\/span>\n  <i class=\"icon-angle-right\" aria-hidden=\"true\" ><\/i><\/a>\n\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n\n\t<div id=\"col-240862142\" class=\"col medium-9 small-12 large-9\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<h2 style=\"text-align: left;\">Prenatal Array and Microarray<\/h2>\n<p>Prenatal array allows us to identify dosage abnormalities (deletions or duplications), heterozygosity, aneuploidies and triploidies in any chromosome region, including those associated with known syndromes and recurring genomic disorders.<\/p>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n<\/div>\n\t\t<\/div>\n\n\t\t\n<style>\n#section_795720642 {\n  padding-top: 50px;\n  padding-bottom: 50px;\n  background-color: rgb(236, 239, 246);\n}\n<\/style>\n\t<\/section>\n\t\n<div class=\"row\"  id=\"row-1159570101\">\n\n\t<div id=\"col-591663312\" class=\"col medium-6 small-12 large-6\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<p>At Sistemas Gen\u00f3micos, we are experts at implementing three types of microarrays: constitutional, prenatal and expression.<\/p>\n<p>Microarrays (also known as molecular karyotype) allow us to detect gains and losses of genetic material with a high resolution and a pan-genomic nature (the study is carried out on the whole genome).<\/p>\n<p>It can be very important to study the expression profile for certain diseases, with special relevance for cancer. RNA arrays allow us to evaluate and compare expression profiles in normal and tumour tissues, in cell cultures treated with a certain form of chemotherapy and without treatment, or to establish which stage of development a certain tissue is at.<\/p>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n\n\t<div id=\"col-1090154643\" class=\"col medium-6 small-12 large-6\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<p>At Sistemas Gen\u00f3micos, we offer the possibility to analyse genetic material from the foetus using and\/or combining different techniques:<\/p>\n<ul>\n<li class=\"bullet-checkmark\">Molecular and conventional cytogenetics: karyotype and FISH.<\/li>\n<li class=\"bullet-checkmark\">Cytogenomics: molecular karyotype using microarray.<\/li>\n<li class=\"bullet-checkmark\">Cytogenetics and oncohaematological FISH.<\/li>\n<\/ul>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n<\/div>\n\t<div id=\"gap-1218779642\" class=\"gap-element clearfix\" style=\"display:block; 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