单词 |
microvillus inclusion disease |
释义 |
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. Synonym(s): congenital microvillus atrophymicrovillus inclusion diseaseA 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 |
随便看 |
- collagen, type i, alpha1
- collagen, type i, alpha 2
- collagen, type i, alpha2
- collagen type ii a-1 gene
- collagen, type ii, alpha1
- collagen type ii alpha-1 gene
- collagen, type iii, alpha 1
- collagen, type iii, alpha1
- collagen type iv a-3 gene
- collagen type iv a-4 gene
- collagen type iv a-5 gene
- collagen type iv alpha-3 gene
- collagen type iv alpha-4 gene
- collagen type iv alpha-5 gene
- collagen, type v, alpha1
- collagen type xi a-1 gene
- collagen type xi a-2 gene
- collagen, type xi, alpha 1
- collagen type xi alpha-1 gene
- collagen type xi alpha-2 gene
- collagen, type xviii, alpha-1
- collagen, type xxi, alpha 1
- collagen vascular disease
- collagen-vascular disease
- collagen vascular disease associated interstitial pneumonia
|