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I just received results of genetic testing after my second miscarriage in a row. I do have one healthy son. Can anyone help me understand what I was told by my doctor? I was told I have a chromasomal abnormality on chromasome #4. I was told that the lower the chromasome abnormality the more the fetus is incompatable with life. I didn't know what questions to ask because I received this information over the phone. My questions are: Is this the main reason that everyone has miscarriages? What is the % of miscarriage from chromasomal abnormalities. Does this mean that if I get pregnant again I can have a chromasomal abnormality on a higher chromasome and it could cause Down Syndrome? Was my firstFirst progesterone mc10 First progesterone mc5 First-progesterone vgs 100 First-progesterone vgs 200 First-progesterone vgs 25 First-progesterone vgs 400 First-progesterone vgs 50 First-testosterone First-testosterone mc child a miracle? I have more questions now then before I knew the results. My doctor didn't suggest coming in to talk to her or genetic testing. I would appreciate any information.
I'm so sorry for your loss! I have read in almost everything written about miscarriage that by far the commonest reason for miscarriage is a chromosomal problem with the fetus. I would ask the doctor to explain whether this #4 is just the testing naming the one that was the problem for this fetus, or if it is considered to be a continued risk. If the doctor doesn't do a satisfactory job of explaining, then you might ask to talk to a genetic counselor. Good luck!
I think I left out that it was a Trisomy on Chromaosome #4. Doctors never tell you enough. I don't know if they think you understand because they do or if they so used to these things happening that it is no big deal to them
majority of m/c are from chromosone abnormality...alot of people who m/c for the first time never really know why because the fetus wasn't sent out for further reasoning....i m/c for the first time in january...my obgyn is very particular with everthing and sent me to a gentic counsulor...i had 69xxx...i had a extra chromosone...the chances of this happening again is less than 1%....you are fine sweetheart!!! if this is your 3 or 4 m/c then i would be concerned..otherwise your fine...babydust and godbless!!
I was a little confused when I read your post because it sounded like you were saying that YOU had a chromosomal abnormality. In fact, after rereading your post, I understand that the fetus (I'm assuming they did genetic testing following the m/c or d&c) had a trisomy of chromosome #4, which led to early miscarriage. This DOES NOT MEAN that you have the same abnormality - if you did, you would not be here (as the doctor said, it is an abnormality incompatible with life). That means that a genetic mutation occurred, probably during cell division (most trisomies occur when DNA replication and cell division don't proceed normally. This doesn't mean that any future fetus would have the same mutation. These mutations are often random events, and chances are you WILL BE FINE the next time. I am frankly shocked that your doctor didn't explain all of this better. I wish you the best and hope this helps you.
- Natalie
Thanks to everyone who responded. I understand that I do not have the same problem. I guess I am confused if this could happen again on a different higher chromosome next time. On a higher chromosome it will live and have extensive problems. I am assuming from the e-mails that this could happen to anyone and that I am not a carrier of anything.
- Natalie