Microvillus inclusion disease, a rare cause of severe congenital diarrhoea;Microvillusinclusieziekte, een zeldzame oorzaak van ernstige aangeboren diarree

Nederlands Tijdschrift voor Geneeskunde

Volumn 146, Issue 31, 2002, Pages 1448-1452

  Jacobs, M J ^a   Tolboom, J J M ^a   Bosman, D K ^a   Van Haelst, U J G M ^a   Bult, P ^a   Kneepkens, C M F ^a   Taminiau, J A J M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DIARRHEA; DISEASE COURSE; DISEASE SEVERITY; ELECTRON MICROSCOPY; FOLLOW UP; HUMAN; INTESTINE BIOPSY; INTESTINE BRUSH BORDER; INTESTINE MUCOSA; INTESTINE TRANSPLANTATION; LIVER TRANSPLANTATION; MALABSORPTION; MICROVILLUS; MICROVILLUS INCLUSION DISEASE; PATHOGENESIS; TOTAL PARENTERAL NUTRITION; CELL INCLUSION; INFANTILE DIARRHEA; NEWBORN; PATHOLOGY; PROGNOSIS; REVIEW; ULTRASTRUCTURE;

ADOLESCENT; DIARRHEA, INFANTILE; DISEASE PROGRESSION; ENGLISH ABSTRACT; HUMAN; INCLUSION BODIES; INFANT, NEWBORN; INTESTINAL MUCOSA; MALABSORPTION SYNDROMES; MICROVILLI; PROGNOSIS; HUMANS;

EID: 0037014822     PISSN: 00282162     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (17)

1. Familial enteropathy: A syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy
2. Familial microvillous atrophy: A clinicopathological survey of 23 cases
3. Microvillus inclusion disease: An inherited defect of brush-border assembly and differentiation
4. Syndrome of intractable diarrhoea with persistent villous atrophy in early childhood: A clinicopathological survey of 47 cases
5. Autoimmune enteropathy and nephropathy with circulating anti-epithelial cell antibodies
6. Tufting enteropathy: A newly recognized clinicopathological entity associated with refractory diarrhea in infants
7. Intractable infant diarrhea associated with phenotypic abnormalities and immunodeficiency
8. The constitutive exocytotic pathway in microvillous atrophy
9. Abnormal expression of brush-border membrane transporters in the duodenal mucosa of two patients with microvillus inclusion disease
10. Biochemical abnormality in brush border membrane protein of a patient with congenital microvillus atrophy
11. Microvillus inclusion disease. In vitro jejunal electrolyte transport
12. Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasia
13. Successful intestinal transplantation for microvillus inclusion disease
14. Combined bowel-liver transplantation in an infant with microvillus inclusion disease
15. Treatment of microvillus inclusion disease by intestinal transplantation
16. Pretransplant management and small bowel-liver transplantation in an infant with microvillus inclusion disease
17. Darmtransplantatie voor behandeling van blijvend darmfalen bij kinderen