Publication:
Congenital microvillus atrophy in a 4-month-old girl

dc.contributor.authorsAcar, Y; Ertem, D; Ozguven, E; Okar, I; Ahiskali, R; Pehlivanoglu, E
dc.date.accessioned2022-03-12T16:58:40Z
dc.date.accessioned2026-01-11T19:25:28Z
dc.date.available2022-03-12T16:58:40Z
dc.date.issued1999
dc.description.abstractCongenital microvillus atrophy is a severe generalized enteropathy with ultrastructural abnormalities of the intestinal brush border. It is a rather new clinicopathological entity which needs to be differentiated from other enteropathies within the spectrum of intractable diarrhea of infancy. The presented case was a four-month-old girl with a chronic, intractable diarrhea, beginning at birth. The diagnosis was established only after the electron microscopic examination of small intestinal mucosa which revealed the characteristic features of the disease. Congenital microvillus atrophy is a rare autosomal recessively inherited disorder and bowel transplantation becomes a realistic option of treatment. Therefore, it should be specifically considered in the differential diagnosis of chronic intractable diarrhea of infancy.
dc.identifier.doidoiWOS:000084848900011
dc.identifier.issn0041-4301
dc.identifier.pubmed10770118
dc.identifier.urihttps://hdl.handle.net/11424/227086
dc.identifier.wosWOS:000084848900011
dc.language.isoeng
dc.publisherTURKISH J PEDIATRICS
dc.relation.ispartofTURKISH JOURNAL OF PEDIATRICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectcongenital microvillus atrophy
dc.subjectintractable diarrhea
dc.subjectinfant
dc.subjectINCLUSION DISEASE
dc.subjectTRANSPLANTATION
dc.subjectDIARRHEA
dc.subjectENTITY
dc.titleCongenital microvillus atrophy in a 4-month-old girl
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage500
oaire.citation.issue4
oaire.citation.startPage495
oaire.citation.titleTURKISH JOURNAL OF PEDIATRICS
oaire.citation.volume41

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