Has anyone else gone through someone similar and if so, what was your results like? Could really use the advice/love/support right now. I am losing my mind over this and really wish we didn't get this test done. Panorama is a Non-Invasive Prenatal Test (NIPT) that screens for common genetic conditions caused by extra or missing chromosomes in the baby’s DNA as early as 9 weeks. The MFM cannot get me in until after I am 16W (per their guideline) and next available appointment isn't until April 7th. OB stated that this could definitely be a lab error or the baby (even myself) is missing an X chromosome or has an extra X or Y chromosome. My OB advised that he has never really seen this with this test (which immediately freaked me out) and suggested next step is to get an ultrasound at an MFM, and from there amniocentesis if needed. The origin of the atypical finding, which involves the X chromosome, could not be specified and may include, but is not limited to, fetal/maternal mosaicism, chromosome abnormality, or normal variation." Repeat cell-free DNA testing is not recommended. No result for sex chromosome abnormalities due to suspected atypical finding. I got my test done at 13W and today received my results, " Atypical finding on sex chromosomes. We also wanted to do this test to determine the gender. When we spoke with our OB at my 12W appointment about the different testing we could do, we figured the genetic and down syndrome testing is good information to know. I have had a rocky pregnancy so far, with bleeding at 5W and 9W but each time the baby has been perfectly healthy. My husband and I found out in January that we were pregnant with our first child (after having a miscarriage in October).
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