Hello all,
I was hoping to share our story and see if anyone else has had a similar issue.
12 week scan was fine, but at 20 week scan (at 21 weeks) the ventricles in the brain were measured at 16mm - severe ventriculomegaly (VM).
We had a more detailed scene with the consultant the next day - the measurements were brought down to 14-15mm - moderate VM.
We were put through for a MRI the following week (22 weeks). This confirmed the VM and put it back at severe, but all other developmental factors appear normal (the silver lining).
We also had amniocentesis and blood tests - so no obvious chromosomal defects, no viral cause, no bleed on the brain. The cause could be a smaller chromosomal error (awaiting genetic assay results), single gene error (not possible to check until after birth) or it could be idiopathic - never to be discovered / known.
We are going in for a full discussion next week, with another scan. But so much is unclear and is based on probability; hard to work with when emotion is so powerful.
So if anyone has any experience please share, support is going to be very important over the next few weeks / months.
Thanks