Are you booked for your 12 week scan? This message is automatically generated for all submissions and might sometimes get it wrong. Rarely, tests results can be false negative, which occur when the results indicate a decreased risk or a genetic condition when the person is actually affected. The main purpose of NIPT is to screen for major chromosome conditions (Down syndrome, trisomy 18, and trisomy 13). Please dont look google to find out. All rights reserved. Hey there, thank you for visiting the sub. This updates the flair on your username IN THIS SUB ONLY. We respect everyones right to express their thoughts and opinions as long as they remain respectful of other community members, and meet What to Expects Terms of Use. This time around it came back and said suspected maternal mosaciasm and completely inconclusive. Like dont they know us preggers are already stressing?!? The waiting is almost unbearable. 3) anything that the NT scan would show (that NIPT wouldnt), the anatomy scan will also show in 20 weeks and that is a standard test for AMA people, as well. This type of result is called uninformative, indeterminate, inconclusive, or ambiguous. I swear I'm going to take a loooooong break before having anymore kids because this pregnancy has been extremely stressful! Do your OB rooms have an on call service you can call? Every sample from a patient is tested to determine whether there is sufficient feto-placental DNA to provide a reliable result. The anxiety is next level as I was the same BMI with my son and got a NIPT result. In cases where the father of the child has not been determined, couples may opt for a, Fetal fraction can be defined as the amount of fetal DNA present in the mothers blood. When did you have your NIPT done? Results in some cases may return inconclusive or uncertain. We just got our results back and have a perfectly healthy . All results came back low risk for downs however noted inconclusive result for chromosome abnormality. 16 week ultrasound scheduled for Monday, June 6 and Amniocentesis scheduled for Wednesday, June 8. If that is all normal I wouldnt worry about this. The #1 app for tracking pregnancy and baby growth. And I'm sick with worry since my first trimester screen came back abnormal. There was another post on here about the same issue. It's new. I hope this helps you consider an alternative, less stressful reason. You could make a big difference by making sure this never happens again in the OB's office for future patients such as yourself. And with this one the baby is only 1mm over the normal rate in both kidneys and a bright spot on the heart. So sorry to hear this is your experience. Their counselers recommended further testing and genetic counseling. Just wondering if anyone has been through something similar :( thanks. 20052023 BabyCenter, LLC, a Ziff Davis company. If there is insufficient fetal DNA. Group Leaders arent expected to spend any additional time in the community, and are not held to a set schedule. So doesnt seem like Im low risk but My obgyn wants to refer me to see a geneticist to discuss possible next steps. I just found out today at 12.5 weeks that my test was not conclusive. Your body then filters it out. Anyone else experienced this? NIPT differs from conventional prenatal screening methods in two important ways. Prediction of other SCA was more accurate. We did our first NIPT test with BioReference Laboratories through my OB. Now I am in limbo awaiting to see what happens next. Don't despair if your grandmother's wisdom turns out to be little more than a good guess. Diagnostic fetal chromosome analysis should be offered after abnormal NIPT or in the presence of cystic hygromas despite normal NIPT. Getting my blood redrawn tomorrow. I'm sure it's just there to drive us insane! That means the results don't indicate for sure whether your baby has a chromosomal condition. I had the first level bloodwork and NT scan and they came back normal. Manal92! Because NIPT consists of a simple blood test, it doesn't create a risk for you or your baby. Group Black's collective includes Essence, The Shade Room and Naturally Curly. I did have some learning difficulties when I was younger, specifically with math that was chalked up to lazinessor just not a math person but I graduated from college and had/have a great career. NIPT does not test for all chromosomal disorders. But higher weight makes NIPT more likely to come back with a "no call" result (although generally not until >180 kg). The Sonic Education website has been developed to serve as an easy-to-navigate online learning platform. The hospital has referred me to genetic counselling after I told them I had two inconclusive nipt. I will keep you all informed about this issue. They all came back negative ! This usually happens when a, Non-Invasive Prenatal Baby Gender Blood Test. The DNA sample of the potential father is collected through a buccal swab, and the two samples are compared to determine paternity. This means that the result is not clear and a result cannot be produced. Canceled due to too many follicles (10 + that were large); BENCHED. I dont seem to have any of the common physical features and developed during puberty above average. The views expressed in community are solely the opinions of participants, and do not reflect those of What to Expect. I hope the baby is growing healthy. Note that once you confirm, this action cannot be undone. Warning: fopen(/nfs/c05/h05/mnt/158483/domains/lomejordelboxeo.com/html/wp-content/uploads/wp-file-manager-pro/fm_backup/.htaccess): failed to open stream: Permission . I think in my case, my first test must have been borderline. Look up their websites and they will tell you the disorders they test for and the accuracy. I am overweight so that may be a contributing factor, although my OB was still very very surprised since she has had very few patients of any size receive an inconclusive result. I just got referred to McMaster as well with a high risk FTS scan/blood work. :). harry hill family. NIPT analyzes fragments of the baby's DNA found circulating in a pregnant person's blood. Group Black's collective includes Essence, The Shade Room and Naturally Curly. Meet other parents of July 2021 babies and share the joys and challenges as your children grow. As of now I have no cardiac or kidney problems but I will see specialists when this baby is born just to be sure. 2) NIPT tests are more accurate and test for MORE genetic disorders (they also tell you sex, if you want to know). Analysis of genes involved in drug metabolism and hypersensitivity, allowing clinicians to prescribe with confidence. It has to be at least above 4 percent to give a conclusive result. My NT ultrasound was normal but they didnt do the blood draw portion because I was getting the nipt, I should ask if they want to do that as well as I may be past the dates for the triple screen draw if I wait for results from my 2nd nipt, Im already 13+2. Group Owners uphold the core values of the brand by reporting content that violates the community guidelines. Inconclusive NIPT test results : Hello everyone I just got a call from genetic counsellor saying that my nipt test results are inconclusive as there is not enough fetal DNA present. Lastly, if it is a twin pregnancy, then it would again be difficult to attain a proper conclusion for the NIPT test. Why genetic testing is bad? In some cases, they will flag a. Best of luck! To complete all the standard tests which came back fine and were able to identify that it was a boy but again, suspect maternal abmormality involving X chromosomes. Use of this site is subject to our terms of use and privacy policy. I had two inconclusive nipt tests at 12 and 13 weeks. She mentioned they might suggest using another company to do the bloodtest (my NIPT were done by lifelab). Negative impact on family and personal relationships. As always, take any information given here and online for what it is - information - and always discuss further treatment plans with your physicians, however with caution. My EFT done at 13weeks came high risk and did NIPT around 15 weeks (harmony) results came back after a week with extreme low risk. Sorry youve gone through this stress xx. I appreciate those who chime in as we all remember how difficult to be in this situation. Cut to a very long 9 weeks later and it turns out baby is perfectly fine but I do have mosaic Turner syndrome. Try not to worry! Just thought I'd update you or anyone else who may read this board. If the concentration of fetal DNA is below this, then the test might prove to be inconclusive. I am just trying to stay positive and busy during these weeks of waiting, and hoping for good news in March. It can be caused by being plus sized.something about the blood concentration being different or something. Reason being: the labs offering these tests seem to only bill people paying out of pocket $250. Both said due to low fetal DNA at 2.6% and 2.7% respectively. So I spent around 5 days suffering because of google. You will see this come up in posts across this sub. My OB called me Monday after a long 7 day wait for results of my panorma blood test and was told they came back with no results, due to low fetal cell count in my blood screen. Yes. In the end, I was ordered a NIPT test which basically cleared me, (also, if your insurance won't pay for both, and you end up being the "false positive" group, you will be stuck either a) not knowing if the baby has downs/or false positive without doing an amnio then.or waiting for much more testing as your pregnancy progresses). We strive to provide you with a high quality community experience. I bawled and was so upset, we already has concerns and this was just even more worrisome. haha our timing for the tests sound quite similar, i am waiting for the referral to see the genetic counselor, so for now will have to wait and see what they recommend. Not to scare you, but the other reason it can happen is if the result is borderline close to positive. the most helpful and trustworthy pregnancy and parenting information. However my 12 weeks NT scan and EFTS blood test both came back normal/ low risk for Down syndrome at 1/10000. We went with Myriad. We are part of Sonic Healthcare, an acknowledged world leader in the provision of diagnostic services, and Australias largest pathology provider. While it is not certain by any means, getting no result during a NIPT test might point toward an increased chance of chromosomal abnormalities. Your post will be hidden and deleted by moderators. No problems and the procedure was not nearly as bad as I thought. Hope you get some answers soon. Luckily, my insurance covered both. Press J to jump to the feed. Please select a reason for escalating this post to the WTE moderators: Connect with our community members by starting a discussion. Contact us today to learn more about everything that we can do for you. I am definitely going to try to stay away from google. Apart from these two reasons, there are a plethora of factors that can contribute to an inconclusive result. No, NIPT is a screening test, not a diagnostic test. Makes me worried about why they can't pick up enough fetal DNA. unfortunately, I called the company and they won't give me any information! You always have a right to speak to a genetic counselor after an abnormal NIPT result and this should be provided for you by your OB. Noninvasive prenatal tests, or NIPTs, screen for an array of rare genetic conditions. I'm waiting on my nipt test results now too. 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