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

Gluten Ataxia?


Keely

Recommended Posts

Keely Newbie

This is confusing.

My 4 year old has severe progressive ataxia (poor walking), and dysarthria (no speech - he signs and is very bright). He has been diagnosed with a mitochondrial disorder and this was what his problems were blamed on.

This spring he had a positive AGA, and went on to get an endoscopy. The endoscopy showed a helicobactor infection, as well as leukocytic infiltrates in the stomach and duodenum, but the villi were fine and celiacs was ruled out for the time being.

We returned for our 6 month appointment and they had more results for us.

Brandon has a positive HLA test, as well as positive TTG, EMA, and AGA.

After doing alot of reading my understanding is gluten ataxia (ataxia and dysarthria mediated by antigluten antibodies attacking the nerves and cerebellum) is a diagnosis that does not require gut involvement.

Does anyone know anything about this diagnosis?

Our GI insists without gut involvement there is no celiacs, however the literature I have found says otherwise.

We are approaching our pediatrician and neurologist about this in the next few days, but im curious if anyone here has any experience.

Thanks in advance,

Keely

www.caringbridge.org/visit/brandonandtyler


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



Celiac.com Sponsor (A8-M):



chrissy Collaborator

i think that both of these can be caused by celiac------which i would say he definitely has if he had a positive TTG and EMA. your son is pretty young still so the gut symptoms may just not be obvious---but if he has a positive TTG, then he has intestinal damage somewhere. those scopes can only go about 6 feet into the small intestine, which means that there is about 16 more feet that they can't test----and the damage can be patchy, so it can be missed by a biopsy.

hopefully, your son's problems are more celiac than mitochondrial.

Guest nini

the biopsies can easily miss damage, and with those specific tests being positive, he does have celiac. and yes it can affect the neurological system instead of the gut, your gi dr. is wrong.

celiacgirls Apprentice

Whatever they call it, it seems your son's problems are at least partly due to gluten. Some doctors won't diagnose celiac without the positive biopsy. Some doctors recognize gluten intolerance as the same thing without the gut damage. Either way, the strict gluten free diet is the answer.

Sophiekins Rookie

It is often the case with neurological celiac disease that the gut is not involved. Print this article: Open Original Shared Link and take it with you to your pediatrician, neurologist and GI. This is written by THE expert on NCD (he discovered gluten ataxia). If you need more help, try posting something on this site: Open Original Shared Link I am pretty sure that there is a mom on there who has had similar experiences, whose son was recently diagnosed with NCD, and if she's not looking, the rest of them are seriously expert and can point you in the right direction from here.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,015
    • Most Online (within 30 mins)
      7,748

    Rockette47
    Newest Member
    Rockette47
    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

    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
    • trents
      @Martha Mitchell, your reaction to the lens implant with gluten sounds like it could be an allergic reaction rather than a celiac reaction. It is possible for a celiac to be also allergic to gluten as it is a protein component in wheat, barley and rye.
    • JoJo0611
    • Martha Mitchell
      Scott I also have different symptoms than most people. It affects me bad. Stomach ache, headache, nauseous, heart racing, whole body shaking, can't walk then my throat starts to close. It attacks my nervous system. The only thing that saves me is a 1/2 of Xanax...it calms down my nervous system 
    • Martha Mitchell
      Scott Adams. I was dealing with a DR that didn't care about me being celiac. I repeatedly told him that I was celiac and is everything gluten-free. He put an acrylic lens from j&j. I called the company to ask about gluten and was told yes that the acrylic they use has gluten....then they back tracked immediately and stopped talking to me. The Dr didn't care that I was having issues. It took me 6 months and a lot of sickness to get it removed.... which can only happen within 6 months. The Dr that took it out said that it was fused and that's why I lost vision. If they would have removed it right away everything would be fine. He put in a silicone one that was gluten-free and I've had no issues at all in the other eye. Do not do acrylic!
×
×
  • 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.