Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

4 Year Old'S Tests All Negative - Now What?


ScootchsMom

Recommended Posts

ScootchsMom Newbie

My 4 year old's test all came back negative, I got copies from the pediatricians office. Her results were:

Gliadin Abs, IgA - 0.7

Gliadin Abs, IgG - 0.8

IGA - 32

TTG IGG - 1

All of her other tests came back as well and while some of her levels are slightly higher than the reference range, or lower in some cases, the peds office said its all normal. Is there anything they missed testing for?

They said they might order allergy tests next week if she is still complaining and still having symptoms.

I'm going to order the Enterolab test to see if that shows anything that the ped isn't catching.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

If the IGA result is her total IGA then she may be IGA deficient which would cause a false negative on tests. It also is known that children have an even higher rate of false negatives than adults do. After all testing is finished do give the diet a good strict try. Please be aware also that celiac is not an allergy and it will not show up on allergy testing.

gf-abis-momma Newbie

My 18 month old has been through so many tests and scopes to find out what is going on with her! All come back saying that she is ok. But if we put her on a gluten diet or have her drink regular milk, life is not fun! The only thing that has worked is the gluten-free diet. Give it a try, no matter what the tests say, it is worth it. If it makes your child feel better, and eases the stress in your life of having a sickchild it is worth it, regardless of what the Dr.'s say. Good luck! hope you get the answers you need. I have resided to the fact that I won't, we just live gluten-free now!

jenny-ann Rookie

Has she had the DNA testing done? Will they do it through your doctor's office? I know our doctor sends it off to Prometheus and bills insurance for us.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,141
    • Most Online (within 30 mins)
      7,748

    Roxyanne18
    Newest Member
    Roxyanne18
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.7k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
    • Skg414228
      Correct. I’m doing both in the same go though. Thanks for clarifying before I confused someone. I’m doing a colonoscopy for something else and then they added the endoscopy after the test. 
    • trents
      It is a biopsy but it's not a colonoscopy, it's an endoscopy.
    • Skg414228
      Well I’m going on the gluten farewell tour so they are about to find out lol. I keep saying biopsy but yeah it’s a scope and stuff. I’m a dummy but luckily my doctor is not. 
    • trents
      The biopsy for celiac disease is done of the small bowel lining and in conjunction with an "upper GI" scoping called an endoscopy. A colonoscopy scopes the lower end of the intestines and can't reach up high enough to get to the small bowel. The endoscopy goes through the mouth, through the stomach and into the duodenum, which is at the upper end of the intestinal track. So, while they are scoping the duodenum, they take biopsies of the mucosal lining of that area to send off for microscopic analysis by a lab. If the damage to the mucosa is substantial, the doc doing the scoping can often see it during the scoping.
×
×
  • Create New...