Multiple m/cs - Greater risk for genetic abnormalities in live birth?
If you've had early recurrent miscarriages, does anyone know if that puts you at greater risk for a live birth with genetic abnormalities? I know I'm getting ahead of myself being just 6w5d and with 10 m/cs (one DD), but I can't get this out of the back of my mind.
As you may know, my bloodwork and ultrasound look great, but I still can't get all happy about it. I also can't stop thinking about the dreaded amnio, and if I should even risk it if this preg progresses...
Thanks. I couldn't find anything online. I'm also 39 which puts me at higher risk. The stress is killing me!
I've had 3 misscarriages in the past and now I'm 26 weeks pregnant with my first child. (through progesterone supplements) I was also worried about the risk of that happening aswell but my gyno assured me that there is absolutely no connection what so ever.
After my dd (and a genetically normal preg before that), I had all the m/cs before 7 weeks (3 were chemical and I just got my period a day or two late). In most, nothing ever grew. Just an empty sac. They were able to test just one preg and it was chromosomally messed up. All my tests came back normal, so we're guessing bad eggs. The only thing that makes my case odd is the first two normal pregs.
I am so hoping that this one grows and is healthy! This is the first time we've seen a heartbeat and everything is the right size.
I asked my RE at Stanford about this today. She said that with each m/c, you have a .1% increase in having a preg with genetic defects than average. So even with 9 early m/cs under my belt (1 was ectopic, so I don't know if that counts) I still have less than a 1% increase risk.
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