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.

Warmly,
Tara

This entry was posted in Uncategorized. Bookmark the permalink.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s