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Diagnosis of Celiac Disease

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Celiac Disease

Part of the book series: Clinical Gastroenterology ((CG))

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Abstract

Patients with celiac disease (CD) can have a variety of different presenting symptoms, ranging from features of intestinal malabsorption to nonclassical features, such as elevated transaminases or osteoporosis, to a silent form of the disease in which villous atrophy is discovered in asymptomatic patients [1, 2]. The diagnosis of CD is currently made through a combination of serological, genetic, and endoscopic testing. The aim of this chapter is to help identify the appropriate patient to test for CD, to review the different serological tests available for the diagnosis of CD, and to discuss the role of genetic testing and endoscopy in the diagnosis of this disease. The diagnosis of CD in children will also be reviewed.

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Tavakkoli, A., Lebwohl, B. (2014). Diagnosis of Celiac Disease. In: Rampertab, S., Mullin, G. (eds) Celiac Disease. Clinical Gastroenterology. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4614-8560-5_9

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