{"id":9260,"date":"2022-07-02T14:48:11","date_gmt":"2022-07-02T12:48:11","guid":{"rendered":"https:\/\/www.new.pbkm.pl\/pregnancy-zone-2\/%pregnancy_zone_category%\/what-does-genetic-testing-consist-of-types-of-genetic-tests-for-children"},"modified":"2022-07-02T14:48:11","modified_gmt":"2022-07-02T12:48:11","slug":"what-does-genetic-testing-consist-of-types-of-genetic-tests-for-children","status":"publish","type":"pregnancy_zone","link":"https:\/\/www.pbkm.pl\/en\/pregnancy-zone-2\/diseases-during-pregnancy\/what-does-genetic-testing-consist-of-types-of-genetic-tests-for-children","title":{"rendered":"What does genetic testing consist of? Types of genetic tests for children"},"content":{"rendered":"<h2 class=\"p1\"><span class=\"s1\"><b>What is genetic testing?<\/b><\/span><\/h2>\n<p class=\"p2\"><span class=\"s2\">Genetic testing is a modern test that focuses on analyzing a person&#8217;s DNA. More and more scientific discoveries confirm that the predisposition to contract certain diseases is genetically determined or arises from mutations. Genetic testing is therefore a valuable diagnostic tool. In&nbsp;depending on the type of test, it can be done in&nbsp;pregnancy or after the birth of the baby.<\/span><\/p>\n<h2 class=\"p1\"><span class=\"s1\"><b>What does genetic testing consist of?<\/b><\/span><\/h2>\n<p class=\"p2\"><span class=\"s2\">Genetic testing involves analyzing a child&#8217;s genetic material. It can be obtained from&nbsp;maternal blood (prenatal testing), from&nbsp;umbilical cord blood or from the infant&#8217;s saliva (tests conducted after the baby is born). Specialists at&nbsp;genetics laboratory then analyze individual genes. The goal of diagnostics is to detect characteristic mutations that are responsible for the predisposition and&nbsp;development of a particular disease. There is usually a wait of several weeks for genetic test results.<\/span><\/p>\n<p><a href=\"https:\/\/www.pbkm.pl\/pregnancy-zone-2\/kurs-okoloporodowy-online-kategoria\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/www.pbkm.pl\/wp-content\/uploads\/2024\/05\/Srodtekstowy_kursokoloporodowy_cartoon.jpg\" alt=\"Srodtext Course v1 1\" width=\"680\" height=\"170\"><\/a><\/p>\n<h2 class=\"p1\"><span class=\"s1\"><b>Comparison of available genetic tests<\/b><\/span><\/h2>\n<p class=\"p3\"><span class=\"s2\">Genetic tests that can be done at&nbsp;to get information about the baby&#8217;s health are:<\/span><\/p>\n<ul style=\"list-style-type: disc;\">\n<li><span class=\"s2\"><br \/>\n  <span class=\"s2\">PlumCare DNA Advisor testing &#8211; after birth&nbsp;<\/span><br \/>\n  <br \/>\n<\/span>PlumCare Advisor DNA genetic testing involves taking a sample of the baby&#8217;s umbilical cord blood or saliva after birth. The material is analyzed at&nbsp;genetics laboratory using the Whole Exome Sequencing (WES) method, that is, the entire exome is examined. This allows for a very accurate genetic assessment and&nbsp;determination of the risk of nearly 300 diseases (predisposition to oncological diseases, metabolic conditions, epilepsy, cardiovascular conditions, connective tissue diseases). The PlumCare DNA Counselor genetic test does not require a blood draw from the mother or baby.&nbsp;<\/li>\n<\/ul>\n<ul style=\"list-style-type: disc;\">\n<li class=\"p4\"><span class=\"s2\">PANORAMA test &#8211; before childbirth<br \/>  The PANORAMA test involves drawing blood from a pregnant woman, and&nbsp;then isolating the baby&#8217;s genetic material from&nbsp;her. It is analyzed for chromosomal abnormalities (trisomies &#8211; Down syndrome, Edwards syndrome, Patau syndrome and&nbsp;triploidies), microdeletions (including cat scream syndrome, Angelman syndrome) and sex chromosome abnormalities (including Turner syndrome, Klinefelter syndrome).&nbsp;<\/span><\/li>\n<li class=\"p4\"><span class=\"s2\">NIFTY test &#8211; before delivery<br \/>  The NIFTY test involves isolating fetal genetic material from&nbsp;the mother&#8217;s blood, and&nbsp;then analyzing it for abnormal chromosome structure. The test can detect the risk of Down, Patau and&nbsp;Edwards syndromes.<\/span><\/li>\n<\/ul>\n<p class=\"p3\"><span class=\"s2\">As you can see, only&nbsp;<a href=\"https:\/\/www.pbkm.pl\/oferta\/badania-genetyczne-plum-care\"><br \/>\n  <span class=\"s3\">PlumCare genetic testing<\/span><br \/>\n<\/a> DNA counselor&nbsp;is performed from&nbsp;umbilical cord blood or saliva of the baby already after birth (i.e., it is completely non-invasive) and&nbsp;allows early detection of predisposition to about 300 severe genetic diseases (the whole genome is analyzed,&nbsp;not individual chromosomes). It is also the only test performed after birth. These are the main differences between the available genetic tests.<\/span><\/p>\n<p class=\"p2\"><span class=\"s2\">Genetic defects can also be detected by prenatal testing, which is a&nbsp;<a href=\"https:\/\/www.pbkm.pl\/pregnancy-zone-2\/jak-dbac-o-siebie-w-ciazy\/jakie-choroby-wykrywa-test-papp-a-kiedy-nalezy-go-wykonac\"><br \/>\n  <span class=\"s3\">PAPP-A test<\/span><br \/>\n<\/a>. The main difference is that the material to be analyzed is not DNA &#8211; the risk of abnormality is determined by the concentration of PAPP-A protein and the free beta-hCG subunit in the pregnant woman&#8217;s blood. They are performed between 11 and&nbsp;14 weeks of pregnancy. Parents-to-be obtain information on whether their child may have trisomies, i.e. Down, Patau or Edwards syndromes, at&nbsp;. It is not possible to determine the predisposition to contract other diseases.<\/span><\/p>\n<p>See also:&nbsp;<a href=\"https:\/\/www.pbkm.pl\/pregnancy-zone-2\/kalendarz-ciazy\/kalendarz-ciazy-12-tydzien-ciazy-jak-rozwija-sie-dziecko\">Pregnancy calendar: 12. One week of pregnancy. How is the child developing?<\/a><\/p>\n<h2 class=\"p1\"><span class=\"s1\"><b>Why is it important to do genetic testing?<\/b><\/span><\/h2>\n<p class=\"p3\"><span class=\"s2\">Many Parents wonder whether it is worthwhile to perform genetic testing on their child. The tests are not reimbursed &#8211; they are carried out only at&nbsp;private facilities, so the decision involves&nbsp;additional expenses. Nevertheless, they provide a lot of valuable information about the toddler&#8217;s health and\/or predisposition to&nbsp;future dangerous and&nbsp;difficult to treat disorders.<\/span><\/p>\n<p class=\"p3\"><span class=\"s3\"><a href=\"https:\/\/www.pbkm.pl\/pregnancy-zone-2\/choroby-w-ciazy\/nieinwazyjne-i-inwazyjne-badanie-prenatalne-w-ciazy-dlaczego-wyniki-tych-badan-sa-istotne-przy-pobieraniu-krwi-pepowinowej\">Genetic prenatal testing<\/a><\/span><span class=\"s2\">&nbsp;make it possible to detect the risk of&nbsp;birth defects and&nbsp;genetic defects even before the child is born. This makes it possible to plan early (or start while still pregnant&nbsp;) treatment and prepare Parents for the possibility of raising a child requiring special care (various therapies and&nbsp;rehabilitation). In&nbsp;some cases, prenatal diagnosis allows termination of pregnancy. These are situations where the detected disease threatens the life of the mother or the fetus.<\/span><\/p>\n<p class=\"p3\"><span class=\"s2\">Postpartum genetic testing has a slightly different task &#8211; it provides knowledge that is broader and&nbsp;complementary to prenatal testing. A pregnancy that went well and the good health of a toddler immediately after birth do not mean that no serious diseases will develop or are not prone to develop in&nbsp;the future. Tests such as the PlumCare DNA Advisor detect such risks before the disease actually occurs. It has two advantages:<\/span><\/p>\n<ul style=\"list-style-type: disc;\">\n<li class=\"p6\"><span class=\"s2\">The possibility of implementing prevention,<\/span><\/li>\n<li class=\"p6\"><span class=\"s2\">and\/or the possibility of starting treatment at an early stage, with a good chance of treatment success.<\/span><\/li>\n<\/ul>\n<p class=\"p3\"><span class=\"s2\">If the Parents are additionally tested, the risk of passing genetic mutations to the child will be determined. About&nbsp;being a carrier of many of&nbsp;them a woman and&nbsp;a man may not even realize.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p class=\"p1\"><span class=\"s1\">One of the&nbsp;cutting-edge genetic tests is PlumCare DNA Advisor. It allows early detection of predisposition to about 300 severe genetic diseases &#8211; mainly metabolic disorders, cardiovascular conditions and&nbsp;oncology. This provides an opportunity to implement preventive measures and&nbsp;appropriate treatment. This type of genetic test can be performed by anyone. All you have to do is apply to the Polish Stem Cell Bank.<\/span><\/p>\n","protected":false},"author":4,"featured_media":7261,"template":"","pregnancy_zone_category":[74],"class_list":["post-9260","pregnancy_zone","type-pregnancy_zone","status-publish","has-post-thumbnail","hentry","pregnancy_zone_category-diseases-during-pregnancy"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Genetic testing - differences. Which ones are best and when to perform?<\/title>\n<meta name=\"description\" content=\"Genetic testing is carried out during pregnancy or after childbirth. 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