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Subject:
From:
Susan Walton <[log in to unmask]>
Reply To:
Susan Walton <[log in to unmask]>
Date:
Wed, 7 Aug 2002 23:56:57 -0400
Content-Type:
text/plain
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<<Disclaimer: Verify this information before applying it to your situation.>>

Original Message:

I had Dr. Fine's gene test done and got the results back via email which =
stated that I had the main gene that predisposes you to Celiac Disease.  =
When I told my ENT about this, he said that he thought that you had to =
have two genes in order to develop CD.  Anyway, my question is, of the =
people on the list who were tested, how many were told they had two =
genes or one gene?  The email that I got said nothing about needing two =
genes to develop CD, but I have read about needing two genes in a couple =
of other places in the past.  Can anyone out there explain this?  Also, =
why did he need a questionnaire filled out about symptoms in order to =
test DNA?  It made me feel a bit like I was giving the answer to the =
question before the test was done. =20

8-7-02
Sorry about the length of this, but since I had so many interesting and =
varied responses, I felt it would be best to post the majority of the =
responses and let you guys decide for yourselves.  My doctor said he =
"thought" you had to have two genes, but was not sure.  He is an ENT and =
he is not treating me for CD.  As far as the test goes, after reading =
the responses, I feel that Dr. Fine would have answered my questions =
since he did this for anyone else who asked.  The reason I did not ask =
was because the email that was sent to me told me to call and set up an =
appointment for a consultation, which I felt would mean even more money. =
  I now know (from reading the responses) that I could have either =
emailed him or called and he would have answered my questions, and =
hopefully, without further charges. =20
     It would have been better to have both an email and a mailed paper =
copy of my gene test with a more thorough explanation of the test =
results.   I now personally feel that he sent the questionnaire for =
research only and he is sincere.   I do not know how I feel about the =
accuracy of the test since we know so little about it.   In my case, I =
can say "yes, it seems to be right", but for others, that may not be the =
case.  Nobody else in my family has ever been diagnosed with CD but I =
have some suspicious family members with lots of symptoms.  We all have =
some of those, I am sure.
---------------------------------
RESPONSES:



I believe if both of your parents have one gene, you will have two genes =
and definitely develop celiac disease. If only one parent has the gene, =
you will have one gene and may still develop celiac disease. Your =
chances would be diminished though.=20
---------------------------


I work for a genecist and in order for the insurance company to pay for =
the testing, reasons need to be given to validate suspicions.  I will =
find out what I can re: the need for one gene or two in celiac disease.. =
 In most diseases we see (not Celiac), both parents need to donate an =
affected gene to create a child with the disease. =20
----------------------
It only takes one gene to develop celiac disease.  Maybe there is more =
of a
likelihood of CD of there are two genes?
I believe the questions are just for statistical purposes.
I tested positive for one gene.  I had the test because of our children =
with
CD, but have not had them genetically tested yet.  I had no symptoms (I
thought) until I went off gluten and realized it made my stomach bloat =
when
I ate gluten.  I have always had a bit of a 'tummy' even though I have
always been thin.  Wish I had known about the gluten connection 20 years
ago. :) I have bad teeth, even though I take care of them, and am a =
little
under average height.
-------------------------------

I believe two genes makes it much more likely that the celiac tendency =
will be triggered.

continued.....

* Visit the Celiac Web Page at www.enabling.org/ia/celiac/index.html *

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