Probably the most proven cell-free DNA-based non-invasive prenatal test (NIPT) 1

Contact Information

Pose a question to your maternity care provider for the Harmony test. You might additionally contact our customer solutions group.

Phone: 1-855-927-4672 (Toll-Free) Call: 1-925-854-6246

What exactly is NIPT?

Non-invasive testing that is prenatalNIPT) uses cell-free DNA (cfDNA) produced from the maternity to gauge feasible chromosomal conditions in a pregnancy. NIPT is really a prenatal assessment test that may be done as soon as 10 days of maternity utilizing a blood draw that is single. Prenatal diagnostic tests such as amniocentesis and CVS diagnose the current presence of chromosomal conditions. These are generally typically done later on in maternity and therefore are connected with a little chance of maternity loss.

Why display for chromosomal conditions?

Chromosomal conditions such as for example Down problem can impact handling of your maternity and distribution as well as the ongoing wellness of one’s newborn.

These conditions sometimes happens in almost any pregnancy- even if there isn’t any 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 created to females under 35 years. 1

That’s why the United states College of Obstetricians and Gynecologists (ACOG) advises that most pregnant women 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 Overseas Society for Prenatal Diagnosis (ISPD) supports providing NIPT to any or all expecting mothers. 3

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.

  1. The California Prenatal Screening Program. March 2009. Company Handbook 2009.
  2. ACOG Practice Bulletin 163 Obstet Gynecol. 2016 May;127(5):e123-37.
  3. Benn et al. Prenat Diagn 2015; 35: 725–734.

For the baby’s health insurance and your reassurance

The Harmony® prenatal test is just a form of NIPT, which could additionally be called NIPS (non-invasive prenatal asian dating testing). It appears at fragments of one’s baby’s DNA in your bloodstream to give information that is accurate the chance for the most typical chromosomal conditions as early as 10 months. It may also recognize the intercourse of the child.

Why display screen for chromosomal conditions?

Chromosomal conditions such as for example Down problem can impact handling of your pregnancy and distribution besides the wellness of the newborn.

These conditions can occur in almost any pregnancy- even if there’s absolutely no grouped family members history- simply because they typically aren’t inherited. They happen by “chance”, and even though the chance increases with mother’s age, many children with chromosomal conditions are born to females under 35 years old. 1

That’s why the United states College of Obstetricians and Gynecologists (ACOG) suggests that most expecting women be provided testing 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 Overseas Society for Prenatal Diagnosis (ISPD) supports providing NIPT to all the expectant mothers. 3

Your prenatal screening results can offer both you and your medical professional with information particular to your maternity in order to have more informed conversations regarding the prenatal care.

  1. The California Prenatal Screening Program. March 2009. Company Handbook 2009.
  2. ACOG Practice Bulletin 163 Obstet Gynecol. 2016 May;127(5):e123-37.
  3. Benn et al. Prenat Diagn 2015; 35: 725–734.

For a selection of conditions

Chromosomal conditions can happen in virtually any maternity. The Harmony test that is prenatal for the most typical ones, including:

  • Trisomy 21 (Down syndrome), trisomy 18 and trisomy 13
  • 22q11.2 microdeletion
  • Monosomy X
  • Intercourse chromosome aneuploidies (SCA)

For three reasons

Clear responses to your concerns

More accurate than old-fashioned testing 2

Less false alarms

Lower false positive rates * than old-fashioned assessment tests 2 *Reports a large probability for a condition when it’s NOT actually present.

Successful by clinical ev >

Evaluated in peer-reviewed magazines involving >148,000 pregnancies in females both under and over age 35 1

Clear responses to your concerns

More accurate than traditional assessment 2

Less false alarms

Lower false positive rates * than conventional testing tests 2 *Reports a big probability for the condition when it’s NOT actually present.

Tested by clinical ev >

Evaluated in peer-reviewed magazines involving >148,000 pregnancies in females both under and over age 35 1

Private stories of three moms and their journeys

Melissa’s Personal tale

I will be the mother of two kids, a child and a son. In the chronilogical age of 40, we became expecting with my 2nd son or daughter, a kid. My spouce and I knew through the outset i might elect to undergo a non-invasive test that is prenatalNIPT). We’d experienced a miscarriage with my very very very first maternity, therefore it had been crucial that you be equipped with because information that is much feasible in regards to the wellness of y our child. We desired to be ready if our infant faced any possible chromosomal conditions.

We were proactive about using a NIPT and I also thought we would just take the Harmony® Prenatal Test, that I discovered from my research, through buddies and my medical practitioner, can be performed because early as 10 days of pregnancy. NIPT appeared like such an improved choice than many other tests which were open to me personally formerly. The test would offer an even more result that is accurate Down problem as compared to older testing tests.

I’ve supported friends that has false positives along with other prenatal assessment practices, therefore precision had been crucial. I’d an experience that is wonderful the Harmony test. It absolutely was effortlessly administered, and we also received the outcomes, which came ultimately back normal, quickly. I think that gathering information during one’s pregnancy is very important. This assessment supplied the information we desired.

Barbara’s Personal tale

I will be a mom to 3 children that are beautiful two on the planet plus one angel who watches over us.

We became expecting with my very very first kid last year and, at that time, non-invasive prenatal screening (NIPT) wasn’t available. I recall this obviously when I discovered of a feasible chromosomal condition during my child from a routine ultrasound and bloodstream test in my own second trimester. My spouce and I confirmed through amniocentesis our daughter that is unborn, had trisomy 18.

We discovered that trisomy 18 is just a rare condition that causes severe variations in development – so serious that many infants with trisomy 18 perish during delivery or fleetingly afterward. Our physician talked about our choices we chose to continue our pregnancy with Joan, knowing the difficult challenges we faced with us, and.

We have experienced two more kiddies since Joan’s death and birth. During those pregnancies, we utilized the Harmony® test that is prenatal. Provided our experience losing our child to trisomy 18, we had been thinking about NIPT for a number of reasons.

The NIPT had been appealing since it’s an easy blood draw – quick, fairly painless, without any danger towards the pregnancy- and it can be performed in the 1st trimester. We knew that when the NIPT outcome had shown a high likelihood for the chromosomal condition, it might have allowed us more hours to get ready for the kid’s unique requirements while the road ahead.

We additionally knew that people didn’t wish to have testing that is invasive a problem ended up being suspected. Both in situations, our Harmony test result indicated that our kids had been unlikely to own three of the most extremely typical chromosome conditions: trisomy 21, trisomy 18 and trisomy 13. Having NIPT when you look at the trimester that is first ease our anxiety for the final two pregnancies. It assisted provide us with some reassurance.

Jean’s Personal tale

I’m sure firsthand essential a noninvasive test that is prenatalNIPT) could be in assisting moms and dads get ready for their infants. While pregnant with my 2nd son I had accepted bloodstream testing with a translucency that is nuchal, therefore the outcomes indicated that my child had a top possibility of being created with Down problem. I happened to be worried sick, and desired more info. The options that are follow-up to my hubby and me are not satisfying to us.

I then found out that the Harmony test has an increased precision compared to the older assessment tests, therefore I asked my physician because of it. We quickly received the outcomes, which indicated that my infant had a rather chance that is low of Down problem, as well as other two conditions tested.

I’m happy to report which our boy that is little is three-years-old and doing great. I’m therefore happy that We thought we would just take the Harmony test. Harmony NIPT to our experience ended up being a good one. I’m glad We took the effort for more information on prenatal testing choices and I also would encourage other expectant mothers to accomplish the exact same in their trimester that is first to very very early responses.

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