So far I've gotten all normal results back from amnio testing and a fetal echo. The genetic counselor mentioned that my MFM dr might want to do a microarray and possibly an eventual MRI. I have another lvl 2 u/s appointment on Friday and I plan to discuss these with him then.

I'm just curious if you've had an amnio and it came back normal, did you pursue further testing? Why or why not?

If you've had a microarray, did they also do a blood study on you and baby's father?


A little background: Baby girl has pleural effusions (fluid in the chest). It is extremely rare to have this and not have an underlying condition.