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{"id":10286,"date":"2019-11-28T01:12:28","date_gmt":"2019-11-27T17:12:28","guid":{"rendered":"http:\/\/www.myfon.com.my\/?p=10286"},"modified":"2019-11-28T01:09:35","modified_gmt":"2019-11-27T17:09:35","slug":"probably-the-most-proven-cell-free-dna-based-non-3","status":"publish","type":"post","link":"https:\/\/www.myfon.com.my\/2019\/11\/28\/probably-the-most-proven-cell-free-dna-based-non-3\/","title":{"rendered":"Probably the most proven cell-free DNA-based non-invasive test that is prenatalNIPT) 1"},"content":{"rendered":"

Probably the most proven cell-free DNA-based non-invasive test that is prenatalNIPT) 1 <\/title> <\/p>\n<h2>Contact Information<\/h2>\n<p>Pose a question to your maternity care provider for the Harmony test. You might additionally contact our customer solutions group. <\/p>\n<p>Phone: 1-855-927-4672 (Toll-Free) Call: 1-925-854-6246<\/p>\n<h2>What exactly is NIPT?<\/h2>\n<p>Non-invasive prenatal screening (NIPT) uses cell-free DNA (cfDNA) produced by the maternity to gauge feasible chromosomal conditions in a maternity. NIPT is just a prenatal assessment test which can be done as soon as 10 months of being pregnant utilizing a blood draw that is single. Prenatal tests that are diagnostic as amniocentesis and CVS diagnose the existence of chromosomal conditions. They’ve been typically done later on in maternity as they are related to a little chance of maternity loss.<\/p>\n<h2>Why display screen for chromosomal conditions?<\/h2>\n<p>Chromosomal conditions such as for example Down problem can impact handling of your maternity and distribution as well as the wellness of the newborn.<\/p>\n<p>These conditions sometimes happens in just about any pregnancy- even if there’s no grouped family members history- simply because they typically aren’t inherited. They happen by “chance”, and even though the chance increases with mom’s age, many children with chromosomal conditions are born to females under 35 years old. 1<\/p>\n<p>That\u2019s why the United states College of Obstetricians and Gynecologists (ACOG) suggests that most expecting women be provided assessment and diagnostic tests for chromosomal conditions. 2 And since NIPT is one of screening that is sensitive for trisomies 21, 18, and 13, the Global Society for Prenatal Diagnosis (ISPD) supports providing NIPT to all or any expecting mothers. 3<\/p>\n<p>Your prenatal screening results can offer both you and information specific to your pregnancy to your doctor in order to do have more informed conversations regarding the prenatal care.<!--more--><\/p>\n<ol>\n<li>The California Prenatal Screening Program. March 2009. Company Handbook 2009.<\/li>\n<li>ACOG Practice Bulletin 163 Obstet Gynecol. 2016 May;127(5):e123-37.<\/li>\n<li>Benn et al. Prenat Diagn 2015; 35: 725\u2013734.<\/li>\n<\/ol>\n<h2>For the baby\u2019s health insurance and your satisfaction<\/h2>\n<p>The Harmony\u00ae prenatal test is a kind of NIPT, which could additionally be called NIPS (non-invasive prenatal testing). It appears at fragments of one’s baby\u2019s DNA in your bloodstream to present information that is accurate the reality for the most typical chromosomal conditions as soon as 10 months. It may also determine the intercourse of the child.<\/p>\n<h2>Why display for chromosomal conditions?<\/h2>\n<p>Chromosomal conditions such as for example Down problem can impact handling of your maternity and distribution besides the wellness of one’s newborn.<\/p>\n<p>These conditions sometimes happens in just about any pregnancy- even though there’s absolutely no family members history- since they typically are not inherited. They happen by “chance”, and though the chance increases with mother’s age, many babies with chromosomal conditions are created to ladies under 35 years old. 1<\/p>\n<p>That\u2019s why the United states College of Obstetricians and Gynecologists (ACOG) suggests that every expecting mothers be provided assessment and diagnostic tests for chromosomal conditions. 2 And because NIPT is considered the most screening that is sensitive for trisomies 21, 18, and 13, the Global Society for Prenatal Diagnosis (ISPD) supports providing NIPT to all or any expectant mothers. 3<\/p>\n<p>Your prenatal screening results can offer you and your medical professional with information particular to your maternity in order to do have more informed conversations regarding the prenatal care.<\/p>\n<ol>\n<li>The California Prenatal Screening Program. March 2009. Company Handbook 2009.<\/li>\n<li>ACOG Practice Bulletin 163 Obstet Gynecol. 2016 May;127(5):e123-37.<\/li>\n<li>Benn et al. Prenat Diagn 2015; 35: 725\u2013734.<\/li>\n<\/ol>\n<h2>For a selection of conditions<\/h2>\n<p>Chromosomal conditions can happen in almost any maternity. The Harmony prenatal test displays for the most frequent ones, including:<\/p>\n<ul>\n<li>Trisomy 21 (Down syndrome), trisomy 18 and trisomy 13<\/li>\n<li>22q11.2 microdeletion<\/li>\n<li>Monosomy X<\/li>\n<li>Intercourse chromosome aneuploidies (SCA)<\/li>\n<\/ul>\n<h2>For three reasons that are good<\/h2>\n<p>Clear responses to the questions you have<\/p>\n<p>More accurate than traditional assessment 2<\/p>\n<p>Less alarms that are false<\/p>\n<p>Lower false positive rates * than conventional testing tests 2 *Reports a high probability for the condition if it is NOT actually present.<\/p>\n<p>Tested by clinical ev ><\/p>\n<p>Evaluated in peer-reviewed magazines involving >148,000 pregnancies in females both under and over age 35 1<\/p>\n<p>Clear responses to your questions<\/p>\n<p>More accurate than old-fashioned testing 2<\/p>\n<p>Less alarms that are false<\/p>\n<p>Lower false positive rates * than conventional testing tests 2 *Reports a large probability for a condition when it’s NOT actually present.<\/p>\n<p>Tested by clinical ev ><\/p>\n<p>Evaluated in peer-reviewed magazines involving >148,000 pregnancies in females both under and over age 35 1<\/p>\n<h2>Private stories of three mothers and their journeys<\/h2>\n<h2>Melissa\u2019s Personal tale<\/h2>\n<p>I’m the caretaker of two kids, a child and a son. A boy at the age of 40, I became pregnant with my second child. We knew through the outset I would personally elect to go through a non-invasive test that is prenatalNIPT). We’d skilled a miscarriage with my very first maternity, so that it ended up being vital that you be equipped with because much information as feasible in regards to the wellness of y our infant. We desired to be ready if our child encountered any prospective chromosomal conditions.<\/p>\n<p>We had been proactive about going for a NIPT and I also thought we would use the Harmony\u00ae Prenatal Test, that we discovered from my research, through buddies and my medical practitioner, can be achieved because early as 10 days of being pregnant. NIPT appeared like such a much better choice than many other tests which were available to me personally formerly. The test would offer an even more accurate outcome for Down problem compared to older testing tests.<\/p>\n<p>I\u2019ve supported friends that has false positives along with other screening that is prenatal, therefore precision had been crucial. I experienced an excellent knowledge about the Harmony test. It had been effortlessly administered, so we received the outcomes, which came ultimately back normal, quickly. I really believe that collecting information during one\u2019s pregnancy is essential. This assessment offered the given information we desired.<\/p>\n<h2>Barbara\u2019s Personal Story<\/h2>\n<p>I will be a mother to three stunning kiddies \u2013 two on the planet and something angel whom watches over us. <\/p>\n<p>We became expecting with my very first son or daughter last year and, at that time, non-invasive prenatal evaluating (NIPT) wasn\u2019t available. From the this demonstrably when I discovered of the chromosomal that is possible in my own child from a routine ultrasound and bloodstream test during my 2nd trimester. We confirmed through amniocentesis which our unborn child, Joan, had trisomy 18.<\/p>\n<p>We discovered that trisomy 18 is just a condition that is rare causes severe variations in development \u2013 so serious that many children with trisomy 18 perish during delivery or fleetingly afterward. Our doctor talked about our choices we chose to continue our pregnancy with Joan, knowing the difficult challenges we faced with us, and.<\/p>\n<p>My spouce and I experienced two more kids since Joan\u2019s death and birth. During those pregnancies, we utilized the Harmony\u00ae prenatal test. Provided our experience losing our child to trisomy 18, we had been thinking about NIPT for many different reasons.<\/p>\n<p>The NIPT had been appealing it can be done in the first trimester as it\u2019s a simple blood draw \u2013 quick, relatively painless, with no risk to the pregnancy- and. We knew that when the NIPT result had shown a high chance for the chromosomal condition, it could have allowed us additional time to get ready for the young child’s unique needs therefore the road ahead.<\/p>\n<p>We additionally knew that people didn\u2019t want testing that is invasive a concern had been suspected. In both cases, our Harmony test result indicated that our kids had been not likely to own three of the most extremely typical chromosome conditions: trisomy 21, trisomy 18 and trisomy 13. Having NIPT into the very first trimester helped relieve our anxiety for the final two pregnancies. It aided provide us with some reassurance.<\/p>\n<h2>Jean\u2019s Personal tale<\/h2>\n<p>I understand firsthand essential a noninvasive test that is prenatalNIPT) may be in assisting moms and dads get ready for their children. While expecting with my second son we had accepted bloodstream testing with a nuchal translucency ultrasound, plus the results indicated that my child had a higher potential for being created with Down problem. I became worried sick, and desired additional information. The options that are follow-up to my hubby and me personally are not satisfying to us.<\/p>\n<p>I consequently found out that the Harmony test has a greater precision than the older testing tests, and so I asked my medical practitioner because of it. We quickly received the outcome, which revealed that my child had a rather low potential for having Down problem, as well as other two conditions tested.<\/p>\n<p>I\u2019m happy to report which our small kid has become three-years-old and doing great. I will be therefore happy that We <a href=\"https:\/\/hot-russian-women.net\/\">ru brides<\/a> made a decision to use the Harmony test. Harmony NIPT to our experience ended up being a confident one. I\u2019m glad We took the initiative for more information on prenatal testing choices and I would encourage other expectant mothers to complete similar throughout their trimester that is first to very early responses.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Probably the most proven cell-free DNA-based non-invasive test that is prenatalNIPT) 1 Contact Information Pose a question to your maternity care provider for the Harmony test. 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