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

Ema Test?


kpyoung24

Recommended Posts

kpyoung24 Rookie

Hi everyone! im new here..... after taking my 7 year old daughter to her pcp with gi symptoms the doc ran two celiac disease tests.. the gliadin and the endomysial(ema) tests. they called two days later with results saying that both tests came back "elevated" and that she probably has celiac but that the diagnosis needs to be confirmed by a gi specialist. i spoke with the gi nurse and she said that the EMA test is pretty specific to celiac disease and that's most likely the diagnosis we are facing but that the gi doc will decide to run the transglutiminase (or however its spelled, lol) test or proceed with the biopsy based on the lab work that the pcp ordered. i guess what im looking for is any info anyone can give me as to whether or not the EMA test is pretty definitive, and if the biopsy is necessary. i know there are many different opinions on this, anything would be appreciated! thanks!!!! kimberly


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



Celiac.com Sponsor (A8-M):



GlutenWrangler Contributor

Kimberly,

The Endomysial Antibody test is very specific for Celiac Disease. Your son's blood test results are conclusive for Celiac Disease. A biopsy is not necessary if you don't want to put your son through it. Some gastroenterologists would just diagnose your son with Celiac Disease with just those test results, and not even bother with a biopsy. A biopsy is useful if you want to determine the level of villi destruction, but it's definitely not necessary at this point for a diagnosis. Hope this helps.

-Brian

kpyoung24 Rookie
Kimberly,

The Endomysial Antibody test is very specific for Celiac Disease. Your son's blood test results are conclusive for Celiac Disease. A biopsy is not necessary if you don't want to put your son through it. Some gastroenterologists would just diagnose your son with Celiac Disease with just those test results, and not even bother with a biopsy. A biopsy is useful if you want to determine the level of villi destruction, but it's definitely not necessary at this point for a diagnosis. Hope this helps.

-Brian

hi brian! thank you very much for your reply! it helps a lot! another question i have is about the biopsy. the tests that were run on my daughter included what the doc referred to as the basic stuff, which she said was like thyroid, elektrolytes etc.... these tests were all "normal", does this indicate that she has little or no villi damage thus far? if so doesn't that make the biopsy completely unnecessary??~K

happygirl Collaborator

The rest of your bloodwork can be fine and your villi can be completely flattened.

The other purpose of an endoscopy is to look for other problems that are causing symptoms.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,065
    • Most Online (within 30 mins)
      7,748

    Hoops
    Newest Member
    Hoops
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Russ H
      This treatment looks promising. Its aim is to provoke immune tolerance of gluten, possibly curing the disease. It passed the phase 2 trial with flying colours, and I came across a post on Reddit by one of the study volunteers. Apparently, the results were good enough that the company is applying for fast track approval.  Anokion Announces Positive Symptom Data from its Phase 2 Trial Evaluating KAN-101 for the Treatment of Celiac Disease https://www.reddit.com/r/Celiac/comments/1krx2wh/kan_101_trial_put_on_hold/
    • Scott Adams
      BTW, we've done other articles on this topic that I wanted to share here (not to condone smoking!):    
    • Colleen H
      Hi everyone  This has been a crazy year so far... How many people actually get entire sensory overload from gluten or something similar ?  My jaw is going nuts ..and that nerve is affecting my upper back and so on ...  Bones even hurt.  Brain fog. Etc  I had eggs seemed fine.   Then my aid cooked a chicken stir fry in the microwave because my food order shorted a couple key items .   I was so hungry but I noticed light breading and some ingredients with SOY !!! Why are we suffering with soy ? This triggered a sensitivity to bananas and gluten-free yogurt it seems like it's a cycle that it goes on.  The tiniest amount of something gets me I'm guessing the tiny bit of breading that I took one tiny nibble of ...yikes ..im cringing from it .. Feels like my stomach is going to explode yet still very hungry 😔  How long does this last?! Thank you so much 
    • Scott Adams
      This is an older article, but may be helpful.  
    • gfmom06
      I have had orthodontic work done. The 3M invisalign material was no problem. BUT my retainers are another matter. They seemed okay for a few months. Now, however, they cause a burning sensation on my tongue, gums and insides of my lips. The burning sensation is now spreading to my throat. I notice it when I breathe. This is annoying and interferes with my enjoyment of eating. I am visiting with my provider tomorrow. We'll see where this goes from here.
×
×
  • 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.