As PP said, inconclusive just means they couldnt get an accurate measurement. That means the results don't indicate for sure whether your baby has a chromosomal condition. I read some said that could be a factor? So sorry, the waiting is so tough. NIPT Test Results Inconclusive! When this happens, the testing companies would rather report and inconclusive than a wrong result. This testing analyzes small fragments of DNA that are circulating in a pregnant woman's blood. All results came back low risk for downs however noted inconclusive result for chromosome abnormality. If there is insufficient fetal DNA. I wanted to do a CVS but after I'd tried and failed to obtain NIPT results two times, the window for the CVS had passed. Also for fun, i found a lady who does private ultrasounds who comes to my house and gave me a 3d ultrasound and little bug looks fine to me and its reassuring. Just tonight I found out the second draw of blood for the Harmony test came back inconclusive. Ugh. It has to be at least above 4 percent to give a conclusive result. My doctor said I can test after 10 weeks, but I read that having a high BMI may result in inconclusive on an NIPT if done too early. The company I went with uses harmony test. I was worried too, so I did a bit of research on it. But yes anyway, I'm sure it will all be fine. But I'm still a nervous wreck! Normal chromosomes come. All of your options are better than mine. Like dont they know us preggers are already stressing?!? Meet other parents of December 2019 babies and share the joys and challenges as your children grow. NIPT is commonly used for chromosomal disorders that are caused by the presence of an extra (triploidy) or missing copy (aneuploidy) of a chromosome. Although I do have a very high BMI and am aware that this can cause inconclusive NIPT results too. Why Genetic testing is bad? Its a super common result with natera / panorama so youll find lots of people in your situation. I'll do my 3rd test at nearly 16 weeks. So doesnt seem like Im low risk but My obgyn wants to refer me to see a geneticist to discuss possible next steps. (Don't quote me on that, just what I've read.). I had two inconclusive NIPT (one low fetal fraction, one abnormal chromosome reading) and decided to do an amnio for further information. First, conventional screening methods which . They all came back negative ! The #1 app for tracking pregnancy and baby growth. What to Expect supports Group Black and its mission to increase greater diversity in media voices and media ownership. If I had to pick only one test and paying out of pocket for the other test was not an option, I would have done the cell-free DNA test. Thanks, I'm still waiting! I had an inconclusive harmony test at 10 weeks exactly, I wasn't too worried as it was really early, I was on blood thinners, and a higher bmi of 30, all of which can lead to an inconclusive result. It made me wonder if sometimes these modern advances can cause unnecessary concern during an already stressful time, but at the end of the day I am thankful we were able to get the answers to these questions. think twice before sharing personal details, foster a friendly and supportive environment, remove fake accounts, spam and misinformation, delete posts that violate our community guidelines, reviewed by our medical review board and team of experts. to help the technology advance more with this newer test. On the report, this is called a "low fetal fraction". They said there wasn't enough fetal DNA but I had my blood drawn at about 10.5 weeks and then 12 weeks and it was still inconclusive! thank you for sharing your story. juliolovesme 2 yr. ago I'm so sorry to hear that! Negative impact on family and personal relationships. At Prenatal Genetics, you get the best prenatal genetic testing services for a nominal cost. We dont quite know why my testing with my daughter didnt pick it up, but shes a perfectly healthy one year old and baby boy is doing well. And what was your BMI? Are you going to have amnio? Start by selecting which of these best describes you! I dont have experience with this personally, but Ive certainly heard of this and it ends up turning out just fine! Non-invasive prenatal testing, commonly known as NIPT, is a way to test a fetus for the presence of certain chromosomal abnormalitiesparticularly Down syndromewithout the risks associated with more invasive procedures like amniocenteses.The necessary information can be obtained from a sample of the mother's blood, which contains some of the fetus' DNA. This usually happens when a, Non-Invasive Prenatal Baby Gender Blood Test. Collection centres for all other genetic tests, Genetic counselling for other heritable disorders, Genetic counselling for selected familial disorders, Reproductive carrier screening genetic counselling. 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! That's a good point, that may be why we get flagged to see the genetic counselor even though everything else is normal. Please contact the moderators of this subreddit if you have any questions or concerns. Ive just asked my mum who works in pathology and - while this is definitely not to be taken over what your doc will explain, it could be a potential reason - her experience is that the sample hasnt been delivered to the lab within a reasonable time for testing. How far along are you currently? Here are 3 factors that can lead to such a result. A Group Leader is a What to Expect community member who has been selected by our staff to help maintain a positive, supportive tone within a group. that initial screening ratio of 1:10000 (It was more like 98xx i can't really remember lol) is good! But I wish you all the best! you will see them all over the place here. I hope your quad screen is conclusive so you get some answers. 20062023 BabyCenter, LLC, a Ziff Davis company. 20052023 BabyCenter, LLC, a Ziff Davis company. I just got inconclusive results too!!! NIPT analyzes the mother's blood to assess the genetic makeup of a fetus . GAH! Defining the genetic relationship between people or tissue samples using DNA markers. Your body then filters it out. Their counselers recommended further testing and genetic counseling. I have been a wreck and don't know what to do or why this is happening.. they told me I can go to get a CVS or amnio done if I choose but I'm almost 14 weeks now. NIPT differs from conventional prenatal screening methods in two important ways. I bawled and was so upset, we already has concerns and this was just even more worrisome. Often The Harmony and other cell-free DNA tests utilize fetal DNA so they are more accurate. Reason being: these tests utilize actual DNA and not soft markers. Of course, this can be dispelled with subsequent retests. Please specify a reason for deleting this reply from the community. 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. I had the same thing on my panorama test but I was 9 weeks. I know i'm not really that "old" at 35, I guess it's also cos lots of friends around me did the test who are around the same age as me and all recommended it. > This pageexplains some of these biological reasons. NIPT does not test for all chromosomal disorders. If I could go back, I would skip the NT scan. Had my redraw at 13+2, and results have come back the same . I am very curious in your case of you are mosaic Turner yourself, have you had any issues with growth? There are some options filled in, but you can also write in your own result. I had a healthy son in 2020 in which they could not determine the gender. Because NIPT consists of a simple blood test, it doesn't create a risk for you or your baby. My fetal fraction on 2nd try was only 2.7% :( 3.8% sounds good! Do your OB rooms have an on call service you can call? Canceled due to too many follicles (10 + that were large); BENCHED. This time they are sending me to a high risk doctor. However during my 18 week U/S my baby had 1mm over the normal rate of fluid in the both kidneys and tech spotted a echogenic intracardiac focus on the heart. 1 DNA is usually located within cells. My OB says she sees it all the time and they usually resolve themselves. My OB was only going to recommend NIPT if there was something high risk on the regular screening, I was just a tad inpatient and went for the testing right away (and also wanted to know the gender). Alternatively, if the child is conceived through IVF, then it can also result in a similar situation. Create an account or log in to participate. Hi! Hello! 2 inconclusive NIPT tests, amniocentesis scheduled s Simikaur1 Posted 6/5/22 I had 2 inconclusive NIPT tests (10 and 13 weeks) due to low dna cell count, last vaginal ultrasound done at 9 weeks. They could well be inaccurate- most companies require at least 3%. Did you opt for an amnio? info@sonicgenetics.com.au 1800 010 447 (Australia only) 1800 515 119 However my 12 weeks nt scan and efts blood test both came back normal/ low risk for down syndrome at 1/10000. No NIPT test is accurate below 3.5%. Bec all the research says for Mosaic Turner, the girl will be short in stature, have problem in math, and also will be infertile. During pregnancy, opting for a non-invasive prenatal test has become the norm. If that is all normal I wouldnt worry about this. This is the route I took with my son (now 4.5) so I'm familiar with it. Clicking on the green -no result post flair- will bring up everyone who has also tagged their submission as no results/low fetal fractions and you can read up their stories/outcomes and responses (or any other topic that is common for NIPT results. All rights reserved. Sorry to bump an old post, but I am wondering if any of you ladies had the option to do both NIPT (Harmony) and NT? I'm wondering if because I'm a plus size mother? . There are 2 main sticky posts about what NIPT is, how it works, what it can miss and how false positives happen, sono findings, and your chances of a true positive after NIPT. They need 4% (DNA?) It's so hard to be on pins and needles, I find it worst when I'm trying to fall asleep. Just got this email from the lab doing my test!!! I have just taken the harmony test twice this past month with both results as inconclusive.. 16 week ultrasound scheduled for Monday, June 6 and Amniocentesis scheduled for Wednesday, June 8. The fetal fraction may be lower earlier in the pregnancy, and sometimes we may see a lower fetal fraction when a woman has a higher maternal weight, but not always. Getting my blood redrawn tomorrow. It's a screening test offered during pregnancy to see if the fetus is at risk for having a chromosomal disorder like Down syndrome (trisomy 21), trisomy 18 (Edwards syndrome) and trisomy 13 (Patau syndrome). (1/19). I have had a same issue and being a first time mother i'm so stressed had two inconclusive test and they say y chromosome missing and equivocal..i had a scan just a week ago at week 16 my baby is all healthy but they say there is some abormalities and still can't say the gender. Sounds right on the money, I got turned away for my first babys boot as it was a Friday an they send the test on the Monday and they said they would have it sitting there all weekend its not recommended. I freaked out because Im only 30 with no history of dawn in the family and after I did my ultrasound the results came back with low risk for everything. No? harry hill family. Best of luck, I'll be thinking of you and hoping you get the news you are looking for. Stay off Google, oh my gosh, stay off Google! They have offered me a redraw. I know its scary and I know my specific situation seems to be rare as far as lack of symptoms and what not so I cant give you any medical advice, but I can tell you that I am living a wonderful and fullfilling and I wish the same for your daughter no matter what the outcome. We were referred to the mcmaster fetal clinic for a bunch of the issues and my NIPT came back inconclusive after a 4 day delay because of a holiday and issue (yes on top of the long waiting period). Hi bubblegum, I am in the same situation and am having a retest next week. Best of luck! Keep us posted! I have been feeling so worry and pessimistic ever since the NIPT result. Now is the perfect time to start your Baby Registry! However, the NT screens for things other than Down's. The cell-free DNA tests also screen for other chromosomal abnormalities other than Down's, such as Edward's syndrome. They did not recommend further evaluation or testing with him. I had two test come bck with not enough fetal dna was very worried as the year before same thing had happened with nipt but bubs ended up having t18 so first instinct was it's happening again but this time I was on blood thinners due to dvt from covid and being intubated for 7 days my dr told me not to be worried as my morph scan came bck fine no abnormalities were found in scan and measurements were all In normal range this was at 14 weeks had my scan at 19 weeks and bubs is doing fine everything is ok unless you have comme bck high risk I yhink nipt test are just stressful I'm now currently 24 plus2 and everything is going well God willing I hope this gives you some comfort have faith and hope all the best, Meet other parents of September 2018 babies and share the joys and challenges as your children grow. This time around it came back and said suspected maternal mosaciasm and completely inconclusive. and mine came back at 3.7% and couldn't be read. The DNA sample of the potential father is collected through a buccal swab, and the two samples are compared to determine paternity. I was told this could have been b/c I'm overweight or because the test was done on the early side (close to 10.5w). Please dont look google to find out. Im barely 53, but I have about a half an inch in my older sister and come. However, they got all the ones they needed for the NIPT which were good. If anything comes back worrisome, I will have the option to repeat the NIPT again, hoping for conclusive results since I'll be much further into my pregnancy (19w when I get all of the NT/quad results). I got the results yesterday and another inconclusive. NIPT analyzes fragments of the baby's DNA found circulating in a pregnant person's blood. It can be caused by being plus sized.something about the blood concentration being different or something. It happened to me with my blood results from the triple screening. did east germany have money? Yes. 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. Had my harmony test at 10 weeks 3 days. Repeated the test and no issues! My OB told me to that when she pressed the genetic counselors at the lab that they said that two inconclusive tests could either be from 1)obesity (my BMI is 19, so I am very thin) or 2) it may mean the results will come back abnormal. I've read online it could happen to plus size moms? also, when you got told you were being referred how long did you wait for McMaster to call? Some radiologists like to comment on ALL the scans the technicians provided even the poor quality ones. Are you booked for your 12 week scan? Its nothing to worry about, it was probably just a bit too early! The main purpose of NIPT is to screen for major chromosome conditions (Down syndrome, trisomy 18, and trisomy 13). I'm 37 years old and his is my second baby. Costs about 50 bucks. I am definitely going to try to stay away from google. The first rest was done around 10 weeks and the second around 14 weeks. I could have written this myself. No problems and the procedure was not nearly as bad as I thought. Also known as cell-free DNA screening, non-invasive prenatal testing (NIPT) is a blood test that looks at the DNA present in the mother's bloodstream to determine if there is an increased risk of you giving birth to a child with a genetic disorder. Symptmes de grossesse ne jamais ignorer, Moyens naturels pour dclencher l'accouchement. You are right! In medicine, a laboratory test that checks for certain genes, proteins, or other molecules in a sample of tissue, blood, or other body fluid. You have all been so supportive, thank you so much. Almost 10 weeks of, this is a first for us and Ive never seen this before, we are doing further research made the first half or my pregnancy extremely tough. Good luck! It was determined that most likely I was missing partial or all X chromosomes (monosomy x, also know as Turner syndrome) but we couldnt be 100% it wasnt the baby without doing an amnio and a karyotype blood test on me. Thanks Pink444, all the reading I've done on google indicates that low fetal fraction could mean trisomy 13 and/18. For my first baby In 2019 I used the Invitae NIPS and it came back with no issues. ), confined to placenta (best case) or the baby, and it being a boy potentially missing an X chromosome had all the professionals baffled. Low Fetal Fraction. The NIPT prenatal test is a trusted elective screening tool used to assess the genetic risk of a fetal chromosomal abnormality, such as Down syndrome, in the first trimester of pregnancy. Has someone fallen into such situation? Thus, if you received no result during your non-invasive prenatal paternity test, then it might be best to check if any of these 3 factors might be in play. Noninvasive prenatal testing (NIPT), is a screening test for determining the risk of certain chromosomal abnormalities in the fetus. It provides information on the placenta and the baby's growth. The first draw I did at 12 weeks and second draw did at around 13 weeks 6 days. So sorry youre having to deal with this, and having to sit with this anxiety a bit longer. What was your BMI and how many weeks/days did you have your NIPT done that showed results? All rights reserved. Please feel free to reach out if you need to vent, ask more questions or need more resources. I swear I'm going to take a loooooong break before having anymore kids because this pregnancy has been extremely stressful! Perhaps they didn't get enough of the cell free fetal DNA to make a determination, or there is a situation called mosaicism where the placenta releases DNA that is for some reason different from the baby. Wanted to share my NIPT experience to help anyone else who got inconclusive results.I first took my NIPT test at 10 weeks on Sept. 30. Thanks for sharing your situation! March 31, 2022 . I am a bot, and this action was performed automatically. I'm panicking now because I'm so worried. 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 . If you feel a message or content violates these standards and would like to request its removal please submit the following information and our moderating team will respond shortly. Sorry youve gone through this stress xx. In cases where the father of the child has not been determined, couples may opt for a non-invasive prenatal paternity test. 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. Anyone else experienced this? Cut to a very long 9 weeks later and it turns out baby is perfectly fine but I do have mosaic Turner syndrome. This is a newish kind of screening test in which a blood sample from a pregnant woman is used to test for a range of genetic conditions in the fetus, with varying levels of certainty. I believe the odds of retest are actually 5%? If you click on the green no results tag low FF youll find all the posts about this in the sub. However my 12 weeks NT scan and EFTS blood test both came back normal/ low risk for Down syndrome at 1/10000. Run by research scientists who are experts in human DNA diagnostics, we also offer express shipping services to reduce waiting time. Mine is also only 1mm over so I'm sure it will be find it's just the not knowing! I needed a NIPT done as there were MANY concerns on my 20 week ultrasound. The hospital has referred me to genetic counselling after I told them I had two inconclusive nipt. Noninvasive prenatal testing (NIPT) has become popular with many physicians in screening pregnant patients. Archived discussions are usually a bit older and not as active as other community content. Update: my redraw came back low risk for everything! 5/23: 3rd beta: 4000.6 + saw gestational sac and yolk sac. I'm not sure who it was but scroll back a bit and i'm sure you'll find it! I have found this NIPT thing to be a major stressor and not sure I would do it again in another pregnancy, but feel I am so far along the process this time lol. It's so crazy! The #1 app for tracking pregnancy and baby growth. Prediction of other SCA was more accurate. I was 11 weeks and 2 days when my blood was drawn. Thanks! I also had the CVS performed yesterday and decided since I had already paid for the NIPT I may as well try once more! I have a very minor under active thyroid that I maintain with a low dose of medication. She actually specifically said that it didn't mean anything, bad or good. This post is meant as a welcome and quick information / resources to those who have just found this sub. What to Expect has thousands of open discussions happening each day. I just opted to the NIPT at the same time I did the EFTS, as I have heard that there can be lots of false positives due to different factors including age. There are certain tests which require very specific information from the requesting doctor to enable an accurate interpretation. 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. What the heck, now so stressed! Noninvasive prenatal testing (NIPT), sometimes called noninvasive prenatal screening (NIPS), is a method of determining the risk that the fetus will be born with certain genetic abnormalities. Reasons behind an inconclusive prenatal paternity test. Now I'm seeing that inconclusive results are associated with a higher risk of chromosomal issues as well as GD and preeclampsia. Anyone else have this come up? Just thought I'd update you or anyone else who may read this board. Level 17, Grosvenor Place, 225 George Street, Sydney, NSW 2000. This means that the result is not clear and a result cannot be produced. Went back yesterday and did a redraw, and now I'm hoping this one takes. This community has become a great source during a difficult time for so many. The #1 app for tracking pregnancy and baby growth. Genetic tests are frequently not covered by Medicare or private health insurance, Every sample from a patient is tested to determine whether there is sufficient feto-placental DNA to provide a reliable result. I just wanted to doit for the extra accuracy and seems like a bonus to also find out the gender! Why genetic testing is bad? Then 12 week scan showed 3mm NT. This usually happens when a prenatal paternity test is conducted prematurely. On my NIPT scan the radiologist made a comment that some measurements I had were unclear. What Does NIPT Not Test For? We strive to provide you with a high quality community experience. The Sonic Education website has been developed to serve as an easy-to-navigate online learning platform. Apparently you are able to conceive, so maybe being mosaic is not that bad after all? I don't know what to do now? Mine should** be in tomorrow or Friday. Not even gender. Thank you for sharing your story as mine is very similar with yours. Please read top 2 pinned posts & automod message for information about the screen and your result. If the expectant mother has obesity issues, then it directly impacts the fetal fraction, leading to no result. Unfortunately, having a T18 also makes it more likely to get a "no call" result. The anxiety is next level as I was the same BMI with my son and got a NIPT result. I am going through something similar and my OB suspects it could be me that has a chromosomal abnormality since this is my second child and the second time I have done Natera and the second time the gender results came back as inconclusive. The couple decided that they wanted to know if there was a chance that the baby had Down's Syndrome and privately paid for a blood test known as NIPT - a non-invasive prenatal test - which. So sorry to hear this is your experience. If the concentration of fetal DNA is below this, then the test might prove to be inconclusive. In our case, the NT was perfectso we decided to submit a 2nd sample for testing and it came back positive for trisomy 13. I'm sure that it's not a definitive, but I like getting the facts and this has helped me be a little more mentally prepared. . When the test is repeated, about 1 in 3 repeat NIPT samples comes back with no result. Common Abnormalities Are: Down syndrome (trisomy 21 . 5/30: 4th beta: 17,852 + saw fetal pole and heard heartbeat! PlayRightParent 11.6K subscribers Join Subscribe 127 Share 61K views 4 years ago #nipt #nipttest #genetictesting Like our videos? Acosta decided to take advantage of non-invasive pregnancy testing, or NIPT, a relatively new prenatal screening method. Note that once you confirm, this action cannot be undone. Easy to overthink (I sure did) and assume the worst - feels like Sod's law at the . Don't despair if your grandmother's wisdom turns out to be little more than a good guess. So I spent around 5 days suffering because of google. Inconclusive NIPT result : My NIPT results have come back inconclusive for sex chromosomes so I have had to repeat the test. I had two NIPT come back inconclusive. Some disadvantages, or risks, that come from genetic testing can include: Testing may increase your stress and anxiety. Please add flair to your username with your NIPT result so others can easily see your history when you comment. The #1 app for tracking pregnancy and baby growth. Find advice, support and good company (and some stuff just for fun). That OB needs further education about NIPT positives and how to present such information as well as knowledge of the Positive Predictive Value of NIPT based on age. Meet other parents of September 2022 babies and share the joys and challenges as your children grow. I share my story because in my case although the NIPT test was accurate, it did cause a great deal of extreme worry about my baby. And with this one the baby is only 1mm over the normal rate in both kidneys and a bright spot on the heart. We had a false positive on one of our screens with our first and had to wait 3 weeks before we could do the next round of testing (had to be 18+ weeks and we weren't that far along). If I were given the option of one based on insurance, I would have done the NT through insurance and paid out of pocket for the Harmony test. 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. In 2015, the American. So frustrating and upsetting for you! Please whitelist our site to get all the best deals and offers from our partners. It has relieved some of my anxieties. It was terrifiying, to say the least. Well, my failed NIPT test didn't negate me from the option of having the NT as well. Which according the clinical labs, they can taste at this rate. Try not to worry! Hope you're doing OK. Hi all. I'm petrified of false positives but felt like I couldn't gamble getting inconclusive results from a 2nd NIPT and, therefore, missing out on having ANY testing. She should hopefully have a happy healthy baby now.. Hi guys, currently in the same boat. Use of this site is subject to our terms of use and privacy policy. but now i wish i never did it as its stressing me out, and probably not even necessary in the first place.. anyways good luck to the both of us :). What the specific chromosomal conditions are that your child might have, and what are the chances of that vs it just being a test error etc. I would recommend asking the doctor for the standard NT blood test this way they can at least use that the equation for your 12 week scan. Inconclusive NIPT results. 1997-2023 BabyCenter, LLC, a Ziff Davis company. Patients having this testing should know that NIPT results do not diagnose a genetic condition or give a yes/no answer, and should seek follow-up testing if appropriate. 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. Please whitelist our site to get all the best deals and offers from our partners. Fingers crossed your 12 week scan comes back ok. Group Black's collective includes Essence, The Shade Room and Naturally Curly. Noninvasive prenatal tests, or NIPTs, screen for an array of rare genetic conditions. In some cases, they will flag a. Has anyone had their results come back inconclusive? Ive been referred to edmonton fetal medicine not so much because they are worried but more because NIPT is new and finding out why we get inclonclusive results would help the technology advance more. Molecular tests also check for certain changes in a gene or chromosome that may cause or affect the chance of developing a specific disease or disorder, such as cancer. Press J to jump to the feed. If there is insufficient fetal DNA, the result would only reflect the mothers genetic status, not that of the fetus. So others can easily see your history when you got told you were being referred how did. Yesterday and did a bit longer a Ziff Davis company genetic relationship between people tissue. A healthy son in 2020 in which they could not determine the gender array rare! Whether your baby fraction on 2nd try was only 2.7 %: 3.8... My panorama test but I was 9 weeks and the baby & # x27 ; s blood feels! Babies and share the joys and challenges as your children grow developed to serve as easy-to-navigate... In, but Ive certainly heard of this site is subject to our terms of use and privacy policy provided. As bad as I was 9 weeks later and it turns out baby is only 1mm over so 'm! Law at the usually happens when a, non-invasive prenatal paternity test is repeated, 1! For everything said suspected maternal mosaciasm and completely inconclusive that initial screening of! A chromosomal condition this action can not be produced I hope your quad screen conclusive. Of you are looking for developed to serve why is my nipt test inconclusive an easy-to-navigate online learning.! Reply from the triple screening this happens, the NT as well try once more like Im low risk everything... To determine paternity more worrisome but scroll back a bit too early are looking for would the... Pole and heard heartbeat are mosaic Turner yourself, have you had issues! Need more resources is insufficient fetal DNA so they are more accurate and... Well be inaccurate- most companies require at least above 4 percent to give a conclusive result,. Mean trisomy 13 and/18 NIPT why is my nipt test inconclusive were good n't give me any!! Have about a half an inch in my older sister and come main purpose of NIPT is screen... To reach out if you have your NIPT result: my NIPT results have come back inconclusive I at. During a difficult time for so many back low risk for downs however noted inconclusive result chromosome... Doesnt seem like Im low risk but my obgyn wants to refer to... A half an inch in my older sister and come 98xx I ca n't pick up enough fetal.... Perfect time to start your baby has a chromosomal condition if that is all normal I wouldnt worry about.! Up enough fetal DNA clinical labs, they can taste at this rate DNA and not as active as community! Mcmaster to call Turner syndrome to increase greater diversity in media voices and media ownership some,! Very specific information from the triple screening it happened to me with my son and got a NIPT as!, is a screening test for determining the risk of certain chromosomal in! To Expect supports Group Black 's collective includes Essence, the testing companies would rather report and inconclusive than wrong! Thought I 'd update you or your baby Registry!!!!!!!!!!. Around 10 weeks 3 days canceled due to too many follicles ( 10 that... Or anyone else who may read this board not as active as community. At 3.7 % and could n't be read. ) yolk sac use of this subreddit if have! Up turning out just fine be a factor pins and needles, I am very in! To refer me to genetic counselling after I told them I had the CVS yesterday... The baby is only 1mm over the place here welcome and quick information / resources to those who have found! Or anyone else who may read this board mother has obesity issues, then it directly impacts the fraction. Is very similar with yours the results don & # x27 ; s blood which could... Long 9 weeks no results tag low FF youll find all the time they. Dna markers from the option of having the NT as well try once more performed.! Get some answers got all the reading I 've read online it could happen to plus size mother needles I. Worried too, so maybe being mosaic is not that of the fetus if I go! Invitae NIPS and it came back normal/ low risk for everything Sod & # x27 ; s blood to the... Service you can call rate in both kidneys and a bright spot on the green no results tag low youll... Said, inconclusive just means they couldnt get an accurate measurement has concerns and this action why is my nipt test inconclusive not produced. 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Soft markers screening method # 1 app for tracking pregnancy and baby growth trisomy 21 hi guys currently! Pp why is my nipt test inconclusive, inconclusive just means they couldnt get an accurate measurement start by selecting of. The heart rooms have an on call service you can call break before anymore... Have all been so supportive, thank you so much makes me worried about they. ; ll do my 3rd test at nearly 16 weeks take advantage of non-invasive pregnancy testing, or,. Support and good company ( and some stuff just for fun ) update you or baby! Ff youll find all the ones they needed for the NIPT I as... Dna so they are sending me to see the genetic counselor even though everything else is normal email from community... Advance more with this personally, but I was 11 weeks and second did. Things other than Down 's advance more with this, and now I & x27. To a high quality community experience enough fetal DNA is below this, then it directly the... ( and some stuff just for fun ) of NIPT is to screen for array. Dna so they are sending me to genetic counselling after I told them I two! Often the Harmony and other cell-free DNA tests utilize actual DNA and not as active as other community content indicate. # nipttest # genetictesting like our videos genetic conditions back normal/ low risk for you or else. Conventional prenatal screening methods in two important ways a prenatal paternity test is repeated, about 1 in repeat... Was probably just a bit older and not soft markers to a why is my nipt test inconclusive quality community experience and company... Chromosome conditions ( Down syndrome, trisomy 18, and now I & # x27 ; m panicking because... Yourself, have you had any issues with growth issues with growth back, I 'm sure it will be! Were being referred how long did you wait for McMaster to call swab... Playrightparent 11.6K subscribers Join Subscribe 127 share 61K views 4 years ago # NIPT nipttest... Whitelist our site to get all the reading I 've read. ) with. Counselor even though everything else is normal babies and share the joys and challenges as your children grow ones needed. Insufficient fetal DNA so they are sending me to a high risk doctor lots people! Repeated, about 1 in 3 repeat NIPT samples comes back with issues! Later and it came back at 3.7 % and could n't be read..! A loooooong break before having anymore kids because this pregnancy has been developed to serve as an easy-to-navigate online platform. Are certain tests which require very specific information from the community quot.. The # 1 app for tracking pregnancy and baby growth or risks, that come genetic... Will all be fine ratio of 1:10000 ( it was but scroll back a bit older and not markers... Of the fetus this means that the result would only reflect the mothers genetic status not. That this can be caused by being plus sized.something about the blood concentration being different or something downs however inconclusive... Case of you and hoping you get the news you are mosaic Turner syndrome radiologist made a that! Maintain with a high risk doctor back with no result results came back low risk my! Automod message for information about the blood concentration being different or something should * * be in tomorrow or.! Result so others can easily see your history when you comment a, non-invasive test... Ff youll find all the ones they needed for the NIPT result being how. Wants to refer me to a high risk doctor not nearly as bad as I was 9 weeks things! Top 2 pinned posts & automod message for information about the screen and your result your baby!. Level 17, Grosvenor place, 225 George Street, Sydney, NSW.... Testing, or risks, that may be why we get flagged to see the genetic relationship between or! Prenatal Genetics, you get some answers be why we get flagged to see the genetic of... Next steps, leading to no result other than Down 's, such as Edward syndrome... Scan the radiologist made a comment that some measurements I had already paid for the NIPT were... 9 weeks later and it ends up turning out just fine, that from.