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

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 may 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 maternity. NIPT is just a prenatal assessment test that may be done as soon as 10 days of being pregnant utilizing a solitary bloodstream draw. Prenatal diagnostic tests such as amniocentesis and CVS diagnose the current presence of chromosomal conditions. They have been typically done later on in maternity and tend to be associated with a tiny threat of maternity loss.

Why display screen for chromosomal conditions?

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

These conditions can occur in almost any pregnancy- even though there isn’t any grouped family members history- since 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 ladies under 35 years. 1

That’s why the United states College of Obstetricians and Gynecologists (ACOG) suggests that most 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 any or all women that are pregnant. 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 your 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 kind of NIPT, that could additionally be called NIPS (non-invasive prenatal assessment). It appears to be at fragments of one’s baby’s DNA in your bloodstream to supply information that is accurate the reality when it comes to most frequent chromosomal conditions as soon as 10 days. It may recognize the intercourse of one’s child.

Why display for chromosomal conditions?

Chromosomal conditions such as for instance Down problem can impact management of your maternity and distribution as well as asian ladys the ongoing wellness of the newborn.

These conditions sometimes happens in every pregnancy- even if there’s absolutely no family members history- since they typically are not inherited. They happen by “chance”, and though the chance increases with mom’s age, many infants with chromosomal conditions are created to females under 35 years old. 1

That’s why the American College of Obstetricians and Gynecologists (ACOG) advises that most expecting women be provided testing and diagnostic tests for chromosomal conditions. 2 And because NIPT is one of screening that is sensitive for trisomies 21, 18, and 13, the Overseas Society for Prenatal Diagnosis (ISPD) supports providing NIPT to all or any expectant mothers. 3

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.

  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 may appear 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 conventional assessment 2

Less false alarms

Lower false positive rates * than old-fashioned testing tests 2 *Reports a big probability for the condition if it is NOT actually present.

Verified 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 conventional testing 2

Less alarms that are false

Lower false positive rates * than conventional testing tests 2 *Reports a large probability for a condition if it is NOT actually present.

Established 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 mothers and their journeys

Melissa’s Personal tale

I will be the caretaker of two kiddies, a child and a son. A boy at the age of 40, I became pregnant with my second child. My spouce and I knew through the outset I would personally elect to go through a non-invasive prenatal test (NIPT). We’d skilled a miscarriage with my very very first maternity, therefore it ended up being crucial that you be armed with because information that is much possible concerning the wellness of y our infant. We wished to additionally be ready if our infant encountered any chromosomal that is potential.

We had been proactive about going for a NIPT and I also thought we would simply take the Harmony® Prenatal Test, that I learned from my research, through buddies and my physician, can be achieved because early as 10 weeks of pregnancy. NIPT appeared like such a much better choice than many other tests that have been open to me personally formerly. The test would offer an even more result that is accurate Down problem as compared to older assessment tests.

I’ve supported friends that has false positives along with other prenatal assessment methods, so precision had been crucial. I experienced an experience that is wonderful the Harmony test. It had been effortlessly administered, and then we received the outcomes, which came ultimately back normal, quickly. I really believe that collecting information during one’s pregnancy is essential. This testing offered the information we desired.

Barbara’s Personal tale

I will be a mom to 3 beautiful kiddies – two on the planet and another angel whom watches over us.

I became expecting with my very very very first kid last year and, at that time, non-invasive prenatal evaluating (NIPT) wasn’t available. I recall this obviously when I discovered of the chromosomal that is possible within my child from the routine ultrasound and bloodstream test within my 2nd trimester. My spouce and I confirmed through amniocentesis which our unborn child, Joan, had trisomy 18.

We discovered that trisomy 18 is just a condition that is rare causes severe variations in development – so serious that a lot of children with trisomy 18 perish during delivery or briefly a short while later. Our medical practitioner talked about our choices we chose to continue our pregnancy with Joan, knowing the difficult challenges we faced with us, and.

My spouce and I have experienced two more kiddies since Joan’s delivery and death. 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 because it’s an easy blood draw – quick, reasonably painless, without any danger to your pregnancy- and it may be performed in the 1st trimester. We knew that when the NIPT result had shown a top chance for a chromosomal condition, it can have allowed us additional time to get ready for the young child’s unique requirements therefore the road ahead.

We additionally knew that individuals didn’t wish to have invasive evaluating unless a problem ended up being suspected. Both in instances, our Harmony test result revealed that our youngsters had been unlikely to possess three of the very most typical chromosome conditions: trisomy 21, trisomy 18 and trisomy 13. Having NIPT within the very first trimester helped relieve our anxiety through the entire final two pregnancies. It aided provide us with some satisfaction.

Jean’s Personal Story

I’m sure firsthand essential a noninvasive test that is prenatalNIPT) could be in assisting moms and dads get ready for their infants. While expecting with my 2nd son we had accepted bloodstream testing having a nuchal translucency ultrasound, and also the outcomes indicated that my infant had a top chance of being created with Down problem. I became worried to the point of sickness, and desired more info. The follow-up choices presented to my hubby and me personally are not satisfying to us.

I then found out that the Harmony test has a greater precision compared to older screening tests, therefore I asked my medical practitioner for this. We quickly received the outcome, which revealed that my child had a rather low possibility of having 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 will be therefore happy that We decided to make the Harmony test. Harmony NIPT to our experience ended up being a confident one. I’m glad We took the initiative for more information about prenatal assessment choices and I also would encourage other expectant mothers to accomplish exactly the same in their trimester that is first to early responses.

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