Severe ventriculomegaly diagnosed at 20 weeks(14 Posts)
I posted this yesterday (copied and pasted below) in the main pregnancy board and was advised to try posting here...has anyone been through something similar to my situation?
"This is where there is excess fluid on the baby's brain, which is usually only picked up at the 20 week scan, not the 12 week scan.
The left ventricule is 7mm which is normal (should be 10mm or under) however the right ventricule is 19mm which is classed as severe.
Waiting for a more in depth/detailed ultrasound with a specialist to see if there are any other abnormalities, however nothing else was picked up on the 20 week scan apart from this excess fluid on the brain and the shape of the head.
Can't help fearing the worst...but hoping there are some positive stories out there?"
We had the detailed ultrasound yesterday and they have picked up further complications as well as confirming the excess fluid on the brain and abnormal shape of the skull which is linked to some syndrome.
We are going ahead with the pregnancy but are unsure of what tests to undergo at the moment.
In a state of absolute shock...has anyone experienced anything similar?
Would really appreciate some advice/support.
We had the same at the 20 week scan. Over the second half of the pregnancy we had lots more scans and were eventually told our son had a skeletal dysplasia. He was born at term. He's had various issues but is now nine and doing well.
No advise or help. But wish you well for your pregnancy! X
Hi sep2299, we are going through a similar thing. Had no complications until the 20 week scan last week that found enlarged ventricles of 18mm and 22mm. Everything else was fine with heart , spine and feutal movements etc. Had the 2nd scan today with a consultant with didn't really tell us much more, just to expect the worst because of the severe size of the ventricles. Blood tests have come back negative for infections and have decided not to to have the chromosome tests. Having an mri this week an meeting with neurosurgeon when get results. Hope things work out for you.
My DD had ventriculomegaly, with measurements of 22 and 24mm at 21 weeks. We had a fetal MRI which confirmed this and showed delayed sulcation (folding) we had Torch analysis (clear), but refused any invasive tests. We were told she had a 95% chance of severe disability. She was born at 34 weeks (unrelated to ventriculomegaly) and after birth an MRI showed her ventricles to be 12 and 16mm. She is now 4 and has no disability or delay. Thinking of you both, it is an incredibly hard thing to go through.
Hi sorry to hear you are going through this.we had bilateral Ventriculomegaly at 20 week scan also ...17mm each side. Worsened to 20mm following week. Amino and infection screen clear. Mri at 23 weeks showed still at 20mm, caused by a blockage ...aqueductal stenosis. Scan at 25 weeks showed no improvement plus midline of brain was now missing that normally separates the 2 sides of brain. Given poor prognosis high risk of disability by 4 consultants. Decided to terminate in the end though very tough decision. It's very hard as docs cannot give you a definite outcome for the child, so all you have is probabilities based on the test results. For us it was a very tough call...this was our 6th IVF so we have longed for a child for a long time and it has not been an easy journey. X
Ventriculomegaly was one of many abnormalities which it was suggested our baby girl may have. Our story was much more complicated and sadly did not have a happy outcome but we learned that scans are not an exact science and were often told one thing and then something completely different. Please feel free to message me if you would like to, I've learned a bit about scans and syndromes along the way and am happy to share
Hi I'm 21 weeks pregnant with my second child and I have been told my son has got bilateral venticallmegally and now next week I'm going for a Fetal MRI on my 20 week scan his left was measuring at 13 mm an his right at 15.3 I don't know what to think or do has anyone been through this could the US be wrong will he live a normal life I jus don't know
He Kelsey, I just stumbled upon your post while looking for information, I am in a similar situation to you, severe ventriculomegaly at 26 weeks. I've had an amnio and MRI, all came back ok which is reassuring, but still leaves unknown factors. Such a terrible time going through those tests though, I have no answers as to what either of us can expect going forward, but I am here to handhold. Good luck with your tests.
Hi I have had my MRI jus waiting on the results glad everything has come back ok and hope everything goes smoothly from now but yeah it is daunting as I don't know what to expect bu fingers crossed everything is all good next week when I get my results but it's the waiting good luck with you and your bundle of joy
Hoping for the best for you. I've been advised that the measurements can change throughout gestation, so with a bit of luck the fluid levels could reduce to within 'normal' range. If the fluid reading is an isolated risk factor then the odds are in our favour that there will be no adverse effects to baby. I am repeating these facts to myself regularly when I feel worried. You've probably been told the same but thought may be worth sharing. Hope results come through soon for you, waiting is hard.
My 3 year old was diagnosed with severe ventriculomegaly at birth which developed into mild hydrocephalus at 5 months. He also has global development delay and cleft lip/palate. Happy to answer any questions you have.
Hi Ellie, thanks for joining us.
I have lots of consultant appointments coming up and have been told this week that baby may need to born early as fluid keeps rising. I'm quite worried now.
How were your results Kelsey?
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