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Diagnosis

To confirm the diagnosis of celiac disease, doctors rely on a combination of blood tests (to look for elevated levels of specific autoantibodies) and small intestine biopsies (to look for characteristic features of celiac disease). These tests must be done while while the patient is still eating a gluten-containing diet. In its Consensus Statement on Celiac Disease, the National Institutes of Health (NIH) has cautioned doctors that, “The single most important step in diagnosing celiac disease is to first consider the disorder.” The NIH issued this warning because symptoms of the disease (e.g., bloating, fatigue, diarrhea, constipation, etc.) could easily blamed on so many other conditions. Indeed, it’s generally believed in the medical community that celiac disease is under-diagnosed in North America – meaning that a lot of people have the disease but don’t realize it. Some studies have estimated that in the U.S., only as few as 1 in 50 or even 1 in 100 cases of celiac disease have actually been diagnosed.
Diagnosing Celiac Disease with Blood Tests and Biopsy
The diagnosis of celiac disease is made with a combination of blood tests and small intestine biopsy.
Genetic Testing for Celiac Disease
Genetic testing for celiac disease might benefit first-degree relatives (parents, children, siblings, grandparents) of celiac patients, people who are already following a gluten-free diet, and people with small intestine biopsy results that are inconclusive.
Dermatitis Herpetiformis
Dermatitis herpetiformis is a painful skin disease caused by an autoimmune reaction to gluten.
Newly Diagnosed? Get a Gluten-Free Care Package
If you or your child has been diagnosed with celiac disease through a biopsy in the past three months, the University of Chicago’s Celiac Disease Center will send you a free basket of gluten-free resources.
Things to Do When Your Child Is First Diagnosed
You need to protect your child from literally thousands of food products. Here are some steps and resources to get you started.

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