Unconclusive

Yep, your guessed it. That option that left us hanging with no knew knowledge? That's what we got. Basically the geneticist said we don't know enough for now, but we've got plans for another MRI at 2 years old, and hope to learn more then.
I mentioned before that this would be the hardest route for me. But I also realize that without a 'label', he also doesn't have a limit. So we're fine with the news (or lack thereof). The doctor gave us the option of doing more random tests to see if we come up with anything, but didn't seem too hopeful that we would. He said the MRI at 2 years old would be our best bet because at 2 more of the brain is developed and you can see any irregularities better.
The only reason we might want to take the chances (and expense) with those random tests is if one of them showed us that he might have a tendency toward a certain ailment and there is something we can do now to help alleviate that.
But for now, he's happy, healthy and learning every day. That's our Easton Experience, and we love it!