Question regarding whole genome testing

I have a question regarding whole genome testing for my son and I.

My son and I both share an immune deficiency that is of yet unsolved. We get infections and don’t create an elevated wcb or it’s a delayed wcb, and it would be great if I could get both of our entire genome sequenced, so we can start by looking at the mutations we share in common.

Is there a way to get an exception for the under 18 rule? Especially since this for his benefit, as much as it is for mine.

Thank for your help.


About hopeforanswers

Some kind of rare immune deficiency, yet to be determined. A lifetime of infections without an elevated white cell blood or fever. Very grateful to be alive, very thankful for the friends who’ve supported me and for access to literally millions of dollars worth of medical care. I’m not the bubble child, I’m somewhere in between.
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