fragile x, anyone?
We were at the neurologist today for a first visit due to DS's migraines, and he took one look at DS, noted that his ears are on the large side and stick out a bit, asked if he had learning disabilities (yes), and said he wanted to do a blood test for Fragile X. I kind of blew it off until I got home and researched it and now I'm a bit freaked out. Many of the symptoms seem to fit. I have no idea how long it will take to get test results. Has anyone dealt with this? Could this be the answer to the LD's, social issues, etc. that we've been dealing with forever?