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Results 1 - 6 of 6 for Congenital microvillous atrophy
  1. ... familial protracted diarrhea with enterocyte brush-border abnormalities Congenital microvillous atrophy Davidson disease Familial protracted enteropathy Intractable diarrhea of ...
  2. ... the MYO5B gene have been found to cause microvillus inclusion disease. This condition is characterized by chronic, life-threatening ... severe diarrhea, malnutrition, and dehydration in individuals with microvillus inclusion disease. More About This Health Condition KIAA1119 MYO5B variant ...
  3. Diarrhea (National Library of Medicine)  
    What is diarrhea? Diarrhea is loose, watery stools (bowel movements). You have diarrhea if you have loose stools three or more times in one day. Acute ...
  4. Digestive Diseases (National Library of Medicine)  
    When you eat, your body breaks food down to a form it can use to build and nourish cells and provide energy. This process is called digestion. Your digestive ...
  5. ... clevelandclinic.org/health/diagnostics/22358-electrolyte-panel Guandalini, S. Microvillus Inclusion Disease Workup. [updated 2017 Oct 06; cited 2024 Mar ...
  6. ... FHL3 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5, WITH OR WITHOUT MICROVILLUS INCLUSION DISEASE; FHL5 PubMed Cetica V, Pende D, Griffiths GM, ...