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Celiac disease
An autoimmune genetic disorder with an unknown pattern of inheritance that primarily affects the digestive tract. It is caused by intolerance to dietary gluten. Consumption of gluten protein triggers an immune response which damages small intestinal villi and prevents adequate absorption of nutrients. Clinical signs include abdominal cramping, diarrhea or constipation and weight loss. If untreated, the clinical course may progress to malnutrition, anemia, osteoporosis and an increased risk of intestinal malignancies. However, the prognosis is favorable with successful avoidance of gluten in the diet.
- Identifiers
- MONDO:0005130 Orphanet:555
- Part of
- Autoimmune disorder of gastrointestinal tractHereditary diseaseMalabsorption syndromeSmall intestine disorder
- Also known as
- celiac sprue · coeliac sprue · gluten intolerance · gluten-induced enteropathy · non tropical sprue
Subtypes
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