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      Frequently Asked Questions About Celiac Disease   09/30/2015

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to Celiac.com's FREE weekly eNewsletter   What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease? - list blood tests, endo with biopsy, genetic test and enterolab (not diagnostic) Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet What if my doctor won't listen to me? An Open Letter to Skeptical Health Care Practitioners Gluten-Free recipes: Gluten-Free Recipes

Would You Pay For Genetic Testing At This Point?
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Diagnosed NCGS. Had full celiac panel done 11mo ago and all was negative. Had positive response to gluten-free diet. Been gluten-free ever since. I have 2 daughters. Both are tiny (as am I), one has constipation issues for sure. My dad was tested for celiac back in the late 80s or early 90s. Result was negative. My mom is pursuing testing because she had a rock bottom B12 and D levels last month and suffers from depression, fatigue, leg aches, etc. I had a follow appt with my doctor today and requested genetic testing. She wouldn't do it. Said it's useless info and that I'm best to do an elimination diet with my kids if I'm concerned (their pediatrician is aware of my diagnosis but hasn't tested girls because they are so young..5 and 2yo).

I'm located in NY. I know I could pay for genetic testing via enterolab and perhaps others. If you were me would you bother? I inquired because I think it would be a helpful piece of the puzzle. If I have genes then a)perhaps I'm a seronegative celiac instead of NCGS and b)if I have genes then I'm more likely to closely monitor and test my daughters. Is that faulty thinking on my part??

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Do keep in mind that usually doctors only check for the two most common celiac associated genes. Just because you might not have those genes doesn't mean you might not be celiac. Also Enterolab testing, last I read, is not available to people living in NY. I was lucky and got my gene testing done through them before NY outlawed it.

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Do keep in mind that usually doctors only check for the two most common celiac associated genes. Just because you might not have those genes doesn't mean you might not be celiac. Also Enterolab testing, last I read, is not available to people living in NY. I was lucky and got my gene testing done through them before NY outlawed it.

Yes, I had the genetic testing and it was negative and I'd tested negative twice to the celiac panel so that was the end of the road formal diagnosis wise for me. Doesn't change the fast that I am extremely intolerant to gluten and I can see that so are other family members. It would've been nice to have those genes so I could get them to go gluten free.

If you can comfortably afford it and are curious then go for it but for me it was really frustrating to have yet another definitive 'no you don't have celiac' strike when I know that I can't touch the stuff. I would've been annoyed if i'd paid for it.

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Thanks for letting me know about the issue of being in NY. Looks like a doc needs to order it in my lovely state. So, I guess it doesn't matter unless I want to shop around for a new doc and find one willing to order it. Bummer.

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Some NY docs will do a stool test via Prometheus for gene testing and it is covered by insurance.

Maybe your doc will do it?

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Some NY docs will do a stool test via Prometheus for gene testing and it is covered by insurance.

Maybe your doc will do it?

I don't think so. She doesn't see the value. It appears that Kimball would do it but would send the results to my doc and I'd need to request a copy from the doc. Pretty sure that's the fastest way to piss off the doc LOL. My mom has a follow up with the doc (we have the same primary care doc) in November to follow up on her bottomed out B12 and I'm pretty sure I have mom convinced to demand celiac testing. Maybe I'll wait to see how that goes before deciding to shop around for another doc.

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Perhaps your Mother's doctor will include genetic testing in her tests. Should hers be positive you would then have reason to ask your doctor again OR if hers are positive it may be enough information for your kids to be genetically tested by their pediatrician.

I was fortunate - when my kids tested negative with symptoms my celiac doc recommended that I have the genetic test. We were all grateful to know that all of my children had at least one celiac gene as it was one less "unknown" in our medical history. My children were teens/young adult when I was diagnosed so the genetic link was important in each of their decisions to pursue more testing &/or go complete a gluten-free trial.

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Do keep in mind that usually doctors only check for the two most common celiac associated genes. Just because you might not have those genes doesn't mean you might not be celiac. Also Enterolab testing, last I read, is not available to people living in NY. I was lucky and got my gene testing done through them before NY outlawed it.

An unnameable company that I tested with, tests for 4 gene alleles. If I have it straight, two of these are celiac and two are gluten intolerance. They also sent explanations that I could understand.

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I don't think so. She doesn't see the value.

I do not see why she even cares one way or the other. You are paying the co-pay for the lab work and all she has to is sign the darn sheet. Geesh. It could be of value to your family.

My doc included it in the first lab work he ran on me. I did not ask for it, he just did it.

"Celiac disease (celiac disease) is a complex genetic disorder with multiple contributing genes. Linkage studies have identified several genomic regions that probably contain celiac disease susceptibility genes. The most important genetic factors identified are HLA-DQ2 and HLA-DQ8, which are necessary but not sufficient to predispose to celiac disease. The associations found in non-HLA genomewide linkage and association studies are much weaker. This might be because a large number of non-HLA genes contributes to the pathogenesis of celiac disease. Hence, the contribution of a single predisposing non-HLA gene might be quite modest. Practically all celiac disease patients carry HLA-DQ2 or HLA-DQ8, while the absence of these molecules has a negative predictive value for celiac disease close to 100%. Genetic risk profiles for celiac disease would be helpful in clinical practice for predicting disease susceptibility and progression."

found here:

http://www.ncbi.nlm.nih.gov/pubmed/18184122

there are others just like this one and I wonder is she would appreciate a few Pub med articles?

:)

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