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

Son's Test Results Returned Normal?


Motherbird7

Recommended Posts

Motherbird7 Rookie

My first child of seven was tested and I requested that they mail me all information. He is my adopted nephew (my side where the celiac family history is) but has no symptoms. His iron was tested normal. But I could not get a clear answer from the doctor as to what was being tested for celiac. The lab tech said they would be running a series of tests so I was hopeful he was getting both IgA and IgG but my lab result says: Celiac Disease Ab Screen w/Rfx ordered AND Celiac Disease Comprehensive cancelled

Is that second one the test I want to have done for my other children some of whom have symptoms?

Anyway here are his results:

Immunoglobulin A, Qn, Serum result: 55 Range: 58-358 Flags: L

We were told by the clinic that his results were negative.

Thank you.


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



Celiac.com Sponsor (A8-M):



frieze Community Regular

My first child of seven was tested and I requested that they mail me all information. He is my adopted nephew (my side where the celiac family history is) but has no symptoms. His iron was tested normal. But I could not get a clear answer from the doctor as to what was being tested for celiac. The lab tech said they would be running a series of tests so I was hopeful he was getting both IgA and IgG but my lab result says: Celiac Disease Ab Screen w/Rfx ordered AND Celiac Disease Comprehensive cancelled

Is that second one the test I want to have done for my other children some of whom have symptoms?

Anyway here are his results:

Immunoglobulin A, Qn, Serum result: 55 Range: 58-358 Flags: L

We were told by the clinic that his results were negative.

Thank you.

if that is all they did, there was no celiac testing done. at. all.

Lisa Mentor

The following are the celiac specific blood tests:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Deamidated Gliadin Peptide (DGP) IgA and IgG

Total Serum IgA

pricklypear1971 Community Regular

And if I'm not mistaken, the only test performed is total iga - and it's below normal - which means he needs be tested with the igg versions of the celiac tests.

Low iga is associated with Celiac disease.

beachbirdie Contributor

My first child of seven was tested and I requested that they mail me all information. He is my adopted nephew (my side where the celiac family history is) but has no symptoms. His iron was tested normal. But I could not get a clear answer from the doctor as to what was being tested for celiac. The lab tech said they would be running a series of tests so I was hopeful he was getting both IgA and IgG but my lab result says: Celiac Disease Ab Screen w/Rfx ordered AND Celiac Disease Comprehensive cancelled

Is that second one the test I want to have done for my other children some of whom have symptoms?

Anyway here are his results:

Immunoglobulin A, Qn, Serum result: 55 Range: 58-358 Flags: L

We were told by the clinic that his results were negative.

Thank you.

Immune globulin A is NOT A CELIAC TEST! What are they doing? Your son is IgA deficient, and as an earlier poster said, he needs to be tested with IgG versions of tests.

Motherbird7 Rookie

I appreciate your responses. I haven't had time to do much research on celiac because I am too busy looking up recipes while figuring out how to eat! lol However, the little I had been able to glean seems to be correct. My daughters have a different doctor so I am hopeful for better communication when they go in tomorrow.

Motherbird7 Rookie

UPDATE:

It looks like I have received more detailed lab results in the mail today for my 13yo son. It appears they did test more than I initially thought but were sent to a LabCorp in NC.

Deamidated Gliadin Abs, IgA: result: 1 range: negative 0-19

t-Transglutaminase (tTg IgA): result: <2 range: negative 0-3

Immunoglobulin A Qn, Serum: result: 55 flag: L range: 58-358

Hemoglobin: 12.8 result: normal range: 11.5-17

So, if I am to understand this....he still needs IgG tested? especially since he is low overall on serum IgA? Or is he okay to accept the negative result for celiac because the tTg IgA is negative which is more celiac specific?

Thanks!


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



Celiac.com Sponsor (A8-M):



MitziG Enthusiast

Because your 13 year old has low IGA, the negative celiac tests are not valid. he has to have IGG testing. As does the 7 year old. That they are both IGA deficient is highly suspicious of celiac as well. Don't let your dr dismiss this. If he will not order the correct tests, find a new dr who is more knowledgeable.

Motherbird7 Rookie

Because your 13 year old has low IGA, the negative celiac tests are not valid. he has to have IGG testing. As does the 7 year old. That they are both IGA deficient is highly suspicious of celiac as well. Don't let your dr dismiss this. If he will not order the correct tests, find a new dr who is more knowledgeable.

Thank you MitziG, I realize I may have caused some confusion. 13yo son is the same one I was originally talking about in this post. He is the first of my seven children, all ages, who will undergo testing. The doctors of the other six children have been receptive to the opinions of those on this forum and have agreed to do the comprehensive celiac panel (still waiting for results on them since they were seen just yesterday and today). Since 13yo has a different doc and was the first to get an appointment, I didn't realize what tests to ask for and apparently his doctor is not as experienced. I will be consulting with her on Monday to see if we can do more bloodwork or take him to one of the other doctors who have been great so far if she is not willing to do it.

Thank you everyone for supporting me through this process!

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. - Florence Lillian replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      13

      gluten free cookie recipes

    2. - Russ H replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    3. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

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

    • Total Members
      132,915
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.