| a hereditary digestive disorder involving intolerance to gluten, usually occurring in young children, characterized by marked abdominal distention, malnutrition, wasting, and the passage of large, fatty, malodorous stools. |
| celiac disease n. A chronic nutritional disturbance, usually of young children, caused by the inability to metabolize gluten, which results in malnutrition, a distended abdomen, muscle wasting, and the passage of stools having a high fat content. The disorder can be controlled by a special diet that emphasizes the elimination of all foods containing gluten. |
celiac disease n.
A malabsorption disease characterized by sensitivity to gluten and atrophy of the mucosa of the upper small intestine, manifested by diarrhea, steatorrhea, and nutritional and vitamin deficiencies. Also called gluten enteropathy, nontropical sprue.
| celiac disease (sē'lē-āk') Pronunciation Key
A gastrointestinal disease characterized by an inability to absorb the protein gluten, resulting in diarrhea, the passage of stools having a high fat content, and nutritional and vitamin deficiencies. Individuals with celiac disease must avoid ingesting products made from grains containing gluten, including wheat, rye, barley, and oats. |