Hello,
My wife is 23 wks pregnant with a girl. A number of days ago we got the results of the amnio fluid test which have shown that the fetus has
turnerTurner syndrome mosaic 45x0/46xx with 30% of abnormal cells. We insisted on doing the FISH test to confirm the result. In the FISH test only 11% of cells (172 cells were tested) were found with
turnerTurner syndrome 45xo, others were
normalNormal saline flush. Since the FISH test is performed directly on the cells taken from the amnio fluid we may assume that this result is more precise than the
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 test that had been performed on cultured cells. It should also be noted that so far the fetus develops absolutely fine and all ultrasound tests done so far were absolutely
normalNormal saline flush with no signs of any kind of patology.
We went to genetic counseling and they explained us the symptoms of
TurnerTurner syndrome syndrom
(syndrome) and told that with the mosaic of 11% the symptoms are expected to be milder (taking into cosideration also that there is nothing abnormal seen on US). Nevertheless, some doctors told us not to take chances and recommeded to stop the pregnancy.
It is a very hard decision to make. My question is: Can anyone tell us what is the probability that our girl will have the symptoms of turner, such as short height, infertility and other problems based on what we know so far - 11% of 45xo and absolutely normal US at 23 weeks. Are there any additional tests that can be done?
Unfortunately we don't have much time, since if we decide to stop the pregnancy it must be done next week.
Thank you in advance,
Alex