microvillus inclusion disease

(redirected from congenital microvillus atrophy)

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.
Farlex Partner Medical Dictionary © Farlex 2012

microvillus inclusion disease

A rare congenital disorder in which newborns or infants develop severe watery diarrhea (caused by intestinal malabsorption) resulting in dehydration, metabolic disarray, and malnutrition. It can be treated with small bowel transplantation when donor organs are available. Synonym: microvillous atrophy
Medical Dictionary, © 2009 Farlex and Partners
References in periodicals archive ?
Indications for the use of HPN in children are short bowel syndrome (SBS), chronic intestinal pseudo-obstruction (CIP), intractable diarrhea, congenital microvillus atrophy, and Crohn's disease (Dahlstrom, Strandvik, Kopple, & Ament, 1985; Ricour, 1989).

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