M
Mommafirst
Guest
Hi Tizzy,
Your situation is exactly what happened with us. The first panel revealed W1282X (not quite as common as the delta F508, but still a well known one) and the docs said she is probably just a carrier. But the extended panel revealed a much more rare mutation. I explained it in my blog, let me get you the link...
<a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/blogpost.cfm?threadid=18463&catid=2131">diagnosis...for a kid with CF</a>
Your situation is exactly what happened with us. The first panel revealed W1282X (not quite as common as the delta F508, but still a well known one) and the docs said she is probably just a carrier. But the extended panel revealed a much more rare mutation. I explained it in my blog, let me get you the link...
<a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/blogpost.cfm?threadid=18463&catid=2131">diagnosis...for a kid with CF</a>