Loss at 10w 5d, No found chromosomal abnormalities in baby — The Bump
Miscarriage/Pregnancy Loss

Loss at 10w 5d, No found chromosomal abnormalities in baby

roberthe10roberthe10 member
Second Anniversary First Comment Photogenic
edited August 2015 in Miscarriage/Pregnancy Loss

I am hoping to find some answers... or comfort in knowing this isn't something I did.

During our first ultrasound, our doctor told us we had a healthy baby measuring 10 weeks, with a heartbeat of 172. We returned for an ultrasound at just about 13 weeks, and were told our little baby no longer had a heartbeat, measuring at 10weeks 5days. The doctor also told us it looked like there was thickening of the neucal folds on the back of her neck, and fluid in her body. That led us to believe she had a chromosomal abnormality. 

The doctor recommended we have genetic testing done on the baby considering our age (DH-28, Me-27), and because we were past 10 weeks. We had the testing and it confirmed she was a girl, we named her Grace, but there were no known chromosomal abnormalities. It has been even harder for me once we found out Grace seemed to be a healthy little baby, but was lost for unknown reasons. Has anyone else experienced a similar situation? Could there have been other things wrong that the genetic testing did not find? 

Re: Loss at 10w 5d, No found chromosomal abnormalities in baby

  • I don't have an answer to your question but I just wanted to say I am sorry for your loss. I think for me having no explanation is the hardest part for me.
    TW: MMC
    BFP1 12/24/14 - EDD 09/07/15 (D/C 8w1d)
    BFP2 6/12/15 - EDD 2/22/16 (D/C 10w3d)
    Diagnoses and Treatments
    PCOS (myo-inositol, excercize)
    Indeterminant levels of APS IgM antibodies (baby aspirin)
    Sub-septate uterus (hysteroscopic septoplasty 12/18/15)
    BFP3 05/02/16 EDD 01/09/17 DS born 01/05/17
    BFP4 01/28/19 EDD 10/?/19 🤞🙏

  • ALC08ALC08 member
    100 Love Its 100 Comments Second Anniversary Name Dropper
    Did you have any other testing? We had genetic test after 1st MC which showed Trisomy 16. After my 2nd MC they did a full panel work up which came back with MTHFR. It is basically a folic acid deficiency. I would probably request further tests. They said they would check for things like clotting disorders, thyroid, and i think lupus. It was very simple, they just took several vials of blood and results were in about a week later.
  • ALC08ALC08 member
    100 Love Its 100 Comments Second Anniversary Name Dropper
    I'm sorry for your loss!!
  • I am so sorry to hear that! I had a MMC with similar timing as yours. A normal genetic test looks at something called a karyotype (is that what they did for you?). If they did a karyotype, then they only look at obvious abnormalities in the chromosomes, like trisomies (or 3 of one chromosome instead of 2), duplications, big chunks of chromosomes missing or extra pieces. As you can imagine, a single change in the DNA/mutations are not detectable this way, your little girls may have had a less obvious genetic defect, if any. 
    I would check with your doctor whether they would like to investigate some more.

    They sent my angel to do genetic testing but no results came back...something about the cells not growing. I really wanted to find out the sex of ours.

    Wish you the best!
    ******TW******Siggy warning
    BFP1 04/24/2015 EDD Dec 2015 MMC 10W5d;
    BFP 2 09/25/2015 EDD June 2016 MMC 9wks; 
    BFP 3 03/22/2016 EDD Dec 6th 2016 

       Baby Birthday Ticker Ticker

  • Thank you for your replies. We have not had any additional testing. The doctor does want us to come in for preconceptual counseling before we decide to try again. I'm assuming they will offer us to have the blood panel workup to check about MTHFR possibilities. Has anyone else been encouraged to have preconceptual counseling after their first loss with no chromosome abnormality findings within the baby?
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