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Microvillus inclusion disease (medical condition): A rare, inherited, progressive intestinal disease where a defect in the intestinal wall results in severe diarrhea after birth.
See also:
Microvillus Inclusion Disease:
»Introduction: Microvillus Inclusion Disease
»Symptoms of Microvillus Inclusion Disease
Microvillus inclusion disease: [MIM*251850] a condition that begins at birth with persistent watery diarrhea and life-threatening malabsorption associated with villous atrophy and crypt hypoplasia in the small bowel; electron microscopy reveals microvillus inclusions in enterocytes. SYN: congenital microvillus atrophy.
Source: Stedman's Medical Spellchecker, © 2006 Lippincott Williams & Wilkins. All rights reserved.
These medical condition or symptom topics may be relevant to medical information for Microvillus inclusion disease:
Microvillus inclusion disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Microvillus inclusion disease, or a subtype of Microvillus inclusion disease,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Microvillus inclusion disease (medical condition): See Microvillus Inclusion Disease (disease information).
»Introduction: Microvillus Inclusion Disease
»Symptoms of Microvillus Inclusion Disease
These medical disease topics may be related to Microvillus inclusion disease:
Source: Diseases Database
Source - NIH
Source: Diseases Database
Search to find out more about Microvillus inclusion disease:
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