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Results 1 - 3 of 3 for Congenital microvillous atrophy
Did you mean Congenital microvillus atrophy?
  1. Microvillus inclusion disease 
    ... familial protracted diarrhea with enterocyte brush-border abnormalities Congenital microvillous atrophy Davidson disease Familial protracted enteropathy Intractable diarrhea of ...
    https://medlineplus.gov/.../condition/microvillus-inclusion-disease - Genetics
  2. MYO5B gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/myo5b - Genetics
  3. Familial hemophagocytic lymphohistiocytosis 
    ... FHL3 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5, WITH OR WITHOUT MICROVILLUS INCLUSION DISEASE; FHL5 PubMed Cetica V, Pende D, Griffiths GM, ...
    https://medlineplus.gov/...milial-hemophagocytic-lymphohistiocytosis - Genetics