I'm 12 weeks and just had my 1st Tri Screen. The nuchal test showed a 10 mm cystic hygroma spanning the length of the fetus, no skull formation, enlarged bladder and a few more developmental issues. Our dr reccomended a 2nd screen on the same day at another location, which showed a 9 mm cystic hygroma, umbilical cord looping including only two outlets instead of three, enlarged bladder, issues with intestinal development and a few other gems. Luckily, the 2nd screen showed skull formation. After speaking with doctors and a genetic counselor we opted for a CVS, which we're waiting for but we have been told that no matter the results of the CVS we're still looking at sever issues and we have at least a 50% chance of miscarrying or carrying a baby to term that had no chance of survival. Can they really tell all of this from a screen? Has anyone had any experience with not only potential chromosomal issues but possible genetic and developmental issues? We're very confused right now as to what to expect.
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