/microvillus inclusion disease

microvillus inclusion disease

Rare Disease

MONDO:0009635

Also Known As

Davidson diseaseMVDMVIDMYO5B secretory diarrheaMYO5B secretory diarrhoeacongenital familial protracted diarrhea with enterocyte brush-border abnormalitiescongenital familial protracted diarrhoea with enterocyte brush-border abnormalitiescongenital microvillous atrophycongenital microvillus atrophydiarrhea 2 with microvillus atrophydiarrhoea 2 with microvillus atrophymicrovillous inclusion diseasemicrovillus inclusion diseasesecretory diarrhea caused by mutation in MYO5Bsecretory diarrhoea caused by mutation in MYO5BDIAR2Davidson's diseasecongenital familial protracted diarrheacongenital familial protracted diarrhea with enterocyte Brush-border abnormalitiescongenital familial protracted diarrhoeacongenital familial protracted diarrhoea with enterocyte Brush-border abnormalitiesdiarrhea 2, with microvillus atrophydiarrhoea 2, with microvillus atrophyfamilial enteropathy, microvillusintractable diarrhea of infancyintractable diarrhoea of infancymicrovillus atrophy, congenital

Definition

Microvillus inclusion disease (MVID) is a very rare, severe, malabsorbative syndrome characterized clinically by protracted or intractable neonatal secretory diarrhea and histologically by inclusion bodies on the intestinal epithelium.