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Screening of Adult/Pediatric Celiac Disease: Early Symptoms and Diagnosis


Screening for adult/pediatric Celiac disease involves testing asymptomatic people for the antibodies to gluten. Americans are not routinely screened for Celiac disease. However, because celiac disease is hereditary, family members--particularly first-degree relatives--of people who have been diagnosed may need to be tested for the disease. About 10 percent of an affected person's first-degree relatives (parents, siblings, or children) will also have the disease. The longer a person goes undiagnosed and untreated, the greater the chance of developing malnutrition and other complications.

Diagnosis of Asymptomatic Celiac Disease and Children

In Italy, where there is a common occurrence of Celiac disease and children are all screened by age 6, even asymptomatic disease is caught early. In addition, Italians of any age are tested for the disease as soon as they show symptoms of Celiac disease candida. As a result of this vigilance, the time between when symptoms begin and the disease is diagnosed is usually only 2 to 3 weeks. In the United States, the time between the first symptoms and diagnosis averages about 10 years.

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