Microvillous inclusion disease: Report of a case with atypical features

Ultrastructural Pathology

Volumn 25, Issue 3, 2001, Pages 275-279

  Mierau, G W ^a   Wills, E J ^a   Wyatt Ashmead, J ^a   Hoffenberg, E J ^a   Cutz, E ^a  

^a CHILDREN S HOSPITAL   (United States)

Author keywords

Electron microscopy; Intestinal microvillous dystrophy; Microvillous inclusion disease

Indexed keywords

ACIDOSIS; ARTICLE; CASE REPORT; CELL INCLUSION; CLINICAL FEATURE; CYTOPLASM; DEHYDRATION; DIARRHEA; DYSTROPHY; ELECTRON MICROSCOPY; ENTEROPATHY; HUMAN; HUMAN TISSUE; INFANT; INTESTINE BIOPSY; INTESTINE BRUSH BORDER; INTESTINE CELL; MALE; MICROVILLUS INCLUSION DISEASE; PRIORITY JOURNAL;

EID: 0034968152     PISSN: 01913123     EISSN: None     Source Type: Journal    
DOI: 10.1080/01913120119148     Document Type: Article

References (16)

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5. Congenital microvillous atrophy: Specific diagnostic features
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8. Siblings with microvillous inclusion disease
9. Enteropathies associated with protracted diarrhea of infancy: Clinicopathological features, cellular and molecular mechanisms
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13. Periodic acid-Schiff staining abnormality in microvillous atrophy: Photometric and ultrastructural studies
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15. A cluster of microvillous inclusion disease in the Navajo population
16. Microvillus inclusion disease: Specific diagnostic features shown by alkaline phosphatase histochemistry