Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.


  • Celiac.com Sponsor (A1):
    Celiac.com Sponsor (A1-M):
  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Celia Gene Test


kcmcc

Recommended Posts

kcmcc Newbie

Does anyone have information on the Celia Gene test? We recently saw a ped. gastro and found out that other test should have been done on our daughter before she went gluten-free. The only test she had was the endomisial antibody test, and now that she is gluten-free I would have to put her on a gluten containing diet to have the biopsy done. She never had any symtoms of celiac. The test was done as a result of another problem she has. I am not comfortable putting back on a gluten containing diet, just to get the biopsy with the chance that she does have celiac. I don't think that is fair to her. The gastro dr. ordered the Celia Gene test. She said that if it comes back negative then does not have celiac, but if is comes back posative it does not mean for sure that she has it either.

Does anyone have any info on this test. As I understand it is fairly new.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Brooke Fried Newbie

I just got off the phone with the celiac research center in Chicago. I was thinking about going there for a biopsy even though I live in florida. I spoke with a nurse who gave me lots of info. The gene test only tells you that you are in a group of people that may have the disease. It is not as clear a test as the biopsy. What they said about the biopsy is right. You have to eat things that are bad so they can look at the intestines and see the damage. Without eating bad things there is no damage, so it won't really tell you much. They say you have to eat gluten for 8 weeks before taking the biopsy which can be very difficult, but it's also very important. And it makes people more strict when they know for sure that what they have is really celiac. it's good to know for sure. That's why I want to do it. You don't have to eat a lot, just a bite of toast every day or anything similar. They recommend a food you don't particularly like so you don't develop any negative feelings.

I am too old to see the famous doctor there, he is a pediatrician (18 and under), but he is known for celiac care. Dr. Guandalini. But you can have the tests anywhere.

Hope that helps.

B

Does anyone have information on the Celia Gene test? We recently saw a ped. gastro and found out that other test should have been done on our daughter before she went gluten-free. The only test she had was the endomisial antibody test, and now that she is gluten-free I would have to put her on a gluten containing diet to have the biopsy done. She never had any symtoms of celiac. The test was done as a result of another problem she has. I am not comfortable putting back on a gluten containing diet, just to get the biopsy with the chance that she does have celiac. I don't think that is fair to her. The gastro dr. ordered the Celia Gene test. She said that if it comes back negative then does not have celiac, but if is comes back posative it does not mean for sure that she has it either.

Does anyone have any info on this test. As I understand it is fairly new.

cherie012 Apprentice

Mason just tested positive for 2 of the celiac genes. the letter states that it is used to RULE OUT celiac if it is negative. Since his was positive, and he has symptoms, we did the scope. Results are pending... For the scope you have to have the gluten, for the blood test looking for the genes, you do not.

Mayam Apprentice

Hi,

Myself and my oldest daughter, who is now 5 1/2, were diagnosed 2 years ago. My middle child had bloodwork done around the same time as our biopsy, she was around 20 mos. Some of her bloodwork came back positive so she also had a biospy, which came back negative. I considered it inconclusive due to her age. I was also not clear on if the ped. GI biopsied more than one part of her intestines. I also have a 14 mo. old son. At our house we are all gluten-free, even my husband who is not a celiac.

I had been wanting to do a genetic test and pay for it out of pocket. However, at one of my celiac support group meetings someone told me about a blood test that runs all the tests you should have to determine celiac disease and if it comes out negative they will automatically test for the genes. I had the test done on my son and middle daughter. Of course their antibody levels were normal since they are gluten-free. They automatically tested their genes and my daughter has two genes and my son has one. I think it was called Celiac Plus panel or something like that. The test is done through Prometheus labs.

I too refuse to put my children on gluten to have a biopsy done. I saw what happened to my oldest before she was diagnosed at 3 1/2 and I will not make my children sick, at least while I'm in control of what they eat.

If your child's test reveals they do not have the gene, they will never develop celiac disease. However, if they are like my kids' tests you will know that they may develop celiac disease sometime during their life.

I think that it is a personal choice as to how to proceed if you receive results that your child does have the gene. (I don't think you stated but if the EMA was positive and the gene is positive it seems that it is assured that your child has celiac disease). I for one, will not give my children gluten and possibly make them sick, especially when they are children and developing so rapidly. When my two younger children are older, at some not yet determined date, I am going to allow them to eat gluten and then observe them. We can worry about their reaction at that time.

Hope this helps you out a bit,

Rachel

daughter age 5

daughter age 3

son age 14 mos.

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to MauraBue's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Have Tru Joy Sweets Choco Chews been discontinued??

    2. - Jmartes71 replied to chrish42's topic in Doctors
      7

      Doctors and Celiac.com

    3. - Wheatwacked replied to MauraBue's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Have Tru Joy Sweets Choco Chews been discontinued??

    4. - Theresa2407 replied to chrish42's topic in Doctors
      7

      Doctors and Celiac.com

    5. - Scott Adams replied to MauraBue's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Have Tru Joy Sweets Choco Chews been discontinued??

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,266
    • Most Online (within 30 mins)
      7,748

    Barbara lynn
    Newest Member
    Barbara lynn
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Scott Adams
      But M&M's contain milk, and would not be at all like a Tootsie Roll.
    • Jmartes71
      I appreciate you validating me because medical is an issue and it's not ok at all they they do this. Some days I just want to call the news media and just call out these doctors especially when they are supposed to be specialist Downplaying when gluten-free when they should know gluten-free is false negative. Now dealing with other issues and still crickets for disability because I show no signs of celiac BECAUSE IM GLUTENFREE! Actively dealing with sibo and skin issues.Depression is the key because thats all they know, im depressed because medical has caused it because of my celiac and related issues. I should have never ever been employed as a bus driver.After 3 years still healing and ZERO income desperately trying to get better but no careteam for celiac other than stay away frim wheat! Now im having care because my head is affected either ms or meningioma in go in tomorrow again for more scans.I know im slowly dying and im looking like a disability chaser
    • Wheatwacked
      M&M Peanuts. About the same calories and sugar while M&M Peanuts have fiber, potassium, iron and protein that Tootsie Rolls ("We are currently producing more than 50 million Tootsie Rolls each day.") don't. Click the links to compare nutritional values.  Both are made with sugar, not high fructose corn syrup.  I use them as a gluten free substitute for a peanut butter sandwich.  Try her on grass fed, pasture fed milk. While I get heartburn at night from commercial dairy milk, I do not from 'grassmilk'.     
    • Theresa2407
      I see it everyday on my feeds.  They go out and buy gluten-free processed products and wonder why they can't heal their guts.  I don't think they take it as a serious immune disease. They pick up things off the internet which is so far out in left field.  Some days I would just like to scream.  So much better when we had support groups and being able to teach them properly. I just had an EMA blood test because I haven't had one since my Doctor moved away.  Got test results today, doctor ordered a D3 vitamin test.  Now you know what  type of doctors we have.  Now I will have to pay for this test because she just tested my D3 end of December, and still have no idea about my EMA.    
    • Scott Adams
      Some of the Cocomels are gluten and dairy-free: https://cocomels.com/collections/shop-page
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.