Hi, Jessica,

we are in the UK and they took blood and it took around 3 months for the
result-but that is if they have the ptpn11 mutation..some noonans kids dont
as there is another one now they know of.

My son Tom was diagnosed and has the ptpn11-but the first time the
genetecist saw him she gave us the diagnosis without reserve..he looks like
a lot of the kids in this group and he is like a twin to a couple of them!

Where did you go for diagnosis? and how old is your son?

kind regards, Linda mum to Tom age 4 ns-a little star!!




>From: "jessica_doty272000" <jessica_doty272000@...>
>Reply-To: noonan_support@yahoogroups.com
>To: noonan_support@yahoogroups.com
>Subject: [noonan_support] can anyone tell we where i can get more info
>about noonans and it's symptoms
>Date: Tue, 19 Sep 2006 00:24:58 -0000
>
>i am needing a little more info about noonans because the doctors
>believe my son has it and when i looked at the pictures of all of the
>kids on here he looks just like them but he hasnt been diagnosed with
>it yet how long does it take to find out for sure
>
>
>