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

1 Year Old Too Young For Endoscopy?


nanderson85

Recommended Posts

nanderson85 Newbie

Hi There, 

I am new here and my DS just had blood work done and it came back positive for Celiac. My husband's sister as well as his cousin have Celiac so I wasn't surprised when the doctor wanted to check him but I am surprised that it came back positive because he does not have any symptoms, that I can tell/know of. I know he is one so he can't tell me how he feels but he isn't upset after eating and poops fairly normally, despite being a bit constipated after switching to cow's milk. I am really wondering if anyone knows how accurate the blood work is in someone his age and also if anyone else has gone through an endoscopy with a child this age. He has been eating solid good since he was 6 months - so about 8 months now - is it too early to see anything in a scope or could there already be damage? I tried researching online, but I only get more confused reading everything and there isn't too much that relates to children his age. Any advice/thoughts are welcome and appreciated! 

Jgapv0RSMvXvprO5G1rYkXG1nWNcniZL_lg.webp


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Welcome to the board.

 

The tests for celiac disease almost always indicate celiac disease.  The rate of false positives is very low, generally below 5%, and those weak positives (often the tTG IgA) are caused by something else like a serious infection, thyroiditis, diabetes, crohns, colitis, and chronic liver disease.  With a family history of celiac disease and no symptoms indicating other diseases, it is celiac disease.

 

This report (pages 10-12) discusses the various tests as well as  a chart (page 12) on the specificity of the disease - specificity means how often a positive is caused by the specific disease (celiac disease).  As you can see, the tests are pretty specific to celiac disease.  If he had more than one positive test, then celiac disease is pretty much a sure thing.  :(  Open Original Shared Link

 

The scope may show damage in him.  In adults, a celiac only needs to eat gluten in the 2-4 weeks prior to the endoscopy to have measurable damage in a biopsy. As long as your son is still consuming gluten, there is a good chance it will be found. Do ensure that at least 6 samples are taken if you choose to have the procedure done; the intestines have a surface area that is the same as a tennis court so if damage is patchy, it can be easy to miss.  

 

If the scope does come back negative, please remember that the scope misses up to 1 in 5 celiacs.  He has already had positive tests so you know he is a celiac no matter what the tests say.

 

Symptoms of celiac disease can be mild.  I was constipated as soon as solids were introduced into my diet.  I started getting stomachaches when I was school aged - it was nothing debilitating but I did lay down and squirm with the pain.  As the years passed my symptoms became more severe but no one figured it out because I was tall and active with C.  Kudos to you for finding this so early and helping him recover.  You'll be saving him years of pain and poor health.

 

This is an interesting article about the usefulness of watching for symptoms in diagnosing celiac disease in kids. Open Original Shared Link

 

Don't forget to retest his siblings and dad every couple of years for life if they continue to eat gluten, sooner if they show symptoms.  Celiac can manifest at any time in life.

 

Best wishes.

nanderson85 Newbie

Thank you for your reply and insight! I feel fortunate that Celiac is something that has been talked about in our family for a few years now so I am familiar with the basics...I know I still have so much to learn though and that worries me a bit. I want to do what is best and right for my son. I also do feel fortunate that it was caught so early, hopefully avoiding a lot of pain for him. We have an appointment with a GI specialist in early November so hopefully they will be able to give me even more insight. I am sure I will be back again with more questions! Thanks again  :)

nvsmom Community Regular

I'm happy to try to help.  :)  Good luck with the GI.  I hope he's a good one and knowledgeable in celiac disease.  Let us know how it goes.

  • 2 weeks later...
calabaza78 Newbie

Just popping in to say that my daughter was diagnosed via blood tests and EGD biopsy at 1 (technically, 21 months.) The report that was written on her biopsy indicated that the specimens did show intestinal damage characteristic of celiac.  

SMRI Collaborator

As far as procedures go, the endoscope is pretty "easy". It's light sedation, quick procedure and usually they will feel 100% shortly after waking up.  I'd do the scope if your dr says just because I know other people who've had issues with getting accommodations and whatnot in school if they are not "biopsy confirmed" Celiac----why, I don't know.  

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. - knitty kitty replied to Scatterbrain's topic in Sports and Fitness
      9

      Feel like I’m starting over

    2. - Scatterbrain replied to Scatterbrain's topic in Sports and Fitness
      9

      Feel like I’m starting over

    3. - knitty kitty replied to Scatterbrain's topic in Sports and Fitness
      9

      Feel like I’m starting over

    4. - knitty kitty replied to Larzipan's topic in Related Issues & Disorders
      34

      Has anyone had terrible TMJ/ Jaw Pain from undiagnosed Celiac?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,311
    • Most Online (within 30 mins)
      7,748

    EMP6543
    Newest Member
    EMP6543
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • knitty kitty
      Check your multivitamin to see if it contains Thiamine Mononitrate, which is a "shelf-stable" form of thiamine that doesn't break down with exposure to light, heat, and time sitting on a shelf waiting to be sold.  Our bodies have difficulty absorbing and utilizing it.  Only 30% is absorbed and less can be utilized.   There's some question as to how well multivitamins dissolve in the digestive tract.  You can test this at home.  YouTube has instructional videos.   Talk to your nutritionist about adding a B Complex.  The B vitamins are water soluble, so any excess is easily excreted if not needed.  Consider adding additional Thiamine in the forms Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) or thiamine hydrochloride.   Thiamine is needed to help control electrolytes.  Without sufficient thiamine, the kidneys loose electrolytes easily resulting in low sodium and chloride.   We need extra thiamine when we're emotionally stressed, physically ill, and when we exercise regularly, are an athlete, or do physical labor outdoors, and in hot weather.  Your return to activities and athletics may have depleted your thiamine and other B vitamins to a point symptoms are appearing.   The deficiency symptoms of B vitamins overlap, and can be pretty vague, or easily written off as due to something else like being tired after a busy day.  The symptoms you listed are the same as early B vitamin deficiency symptoms, especially Thiamine.  Thiamine deficiency symptoms can appear in as little as three days.  I recognize the symptoms as those I had when I was deficient.  It can get much worse. "My symptoms are as follows: Dizziness, lightheaded, headaches (mostly sinus), jaw/neck pain, severe tinnitus, joint stiffness, fatigue, irregular heart rate, post exercise muscle fatigue and soreness, brain fog, insomnia.  Generally feeling unwell." I took a B 50 Complex twice a day and extra thiamine in the forms Benfotiamine and TTFD.  I currently take the Ex Plus supplement used in this study which shows B vitamins, especially Thiamine B 1, Riboflavin B2, Pyridoxine B 6, and B12 Cobalamine are very helpful.   A functional evaluation of anti-fatigue and exercise performance improvement following vitamin B complex supplementation in healthy humans, a randomized double-blind trial https://pmc.ncbi.nlm.nih.gov/articles/PMC10542023/
    • Scatterbrain
      I am taking a multivitamin which is pretty bolstered with B’s.  Additional Calcium, D3, Magnesium, Vit C, and Ubiquinol.  Started Creapure creatine monohydrate in June for athletic recovery and brain fog.  I have been working with a Nutritionist along side my Dr. since February.  My TTG IGA levels in January were 52.8 and my DGP IGA was >250 (I don’t know the exact number since it was so high).  All my other labs were normal except Sodium and Chloride which were low.  I have more labs coming up in Dec.  I make my own bread, and don’t eat a lot of processed gluten-free snacks.
    • knitty kitty
      @Scatterbrain, What supplements are you taking? I agree that the problem may be nutritional deficiencies.  It's worth talking to a dietician or nutritionist about.   Did you get a Marsh score at your diagnosis?  Was your tTg IgA level very high?  These can indicate more intestinal damage and poorer absorption of nutrients.   Are you eating processed gluten free food stuffs?  Have you looked into the Autoimmune Protocol Diet?  
    • knitty kitty
      Vitamin and mineral deficiencies can make TMJ worse.  Vitamins like B12 , Thiamine B1, and Pyridoxine B6 help relieve pain.  Half of the patients in one study were deficient in these three vitamins in one study below. Malabsorption of vitamins and minerals is common in celiac disease.  It's important to eat healthy nutrient dense diets like the Autoimmune Protocol Diet, a Paleo diet that has similarities to the Mediterranean diet mentioned in one of the studies.   Is there a link between diet and painful temporomandibular disorders? A cross-sectional study https://pmc.ncbi.nlm.nih.gov/articles/PMC12442269/   Nutritional Strategies for Chronic Craniofacial Pain and Temporomandibular Disorders: Current Clinical and Preclinical Insights https://pmc.ncbi.nlm.nih.gov/articles/PMC11397166/   Serum nutrient deficiencies in the patient with complex temporomandibular joint problems https://pmc.ncbi.nlm.nih.gov/articles/PMC2446412/  
    • Iam
      Yes.  I have had the tmj condition for 40 years. My only help was strictly following celiac and also eliminating soy.  Numerous dental visits and several professionally made bite plates  did very little to help with symptoms
×
×
  • 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.