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dc.contributor.authorArslanoglu, Sertac
dc.contributor.authorGulluoglu, Mine
dc.contributor.authorAhishali, Bulent
dc.contributor.authorBulut, Ozgul
dc.date.accessioned2021-03-04T08:53:33Z
dc.date.available2021-03-04T08:53:33Z
dc.date.issued2017
dc.identifier.citationBulut O., Ahishali B., Gulluoglu M., Arslanoglu S., "A Case Study of Intractable Diarrhea Due to Neonatal Microvillous Inclusion Disease", FETAL AND PEDIATRIC PATHOLOGY, cilt.36, sa.4, ss.340-343, 2017
dc.identifier.issn1551-3815
dc.identifier.otherav_6589bc14-048f-4bd8-802f-8ee986a31550
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/70595
dc.identifier.urihttps://doi.org/10.1080/15513815.2017.1333178
dc.description.abstractBackground: Microvillous inclusion disease (MVID) is one of the most severe congenital diarrhea disorders, caused by a genetic defect in enterocyte differentiation and polarization. Case report: We describe a neonate who presented with severe weight loss, hypernatremic dehydration and metabolic acidosis due to intractable diarrhea due to MVID, confirmed by electron microscopy. Conclusion: MVID can present with severe weight loss, hypernatremic dehydration and metabolic acidosis that is life threatening. The diagnosis is made by typical findings on light microscopy and electron microscope of small bowel biopsies. The only therapeutic options at this time are total parenteral nutrition and bowel rest and intestinal transplantation.
dc.language.isoeng
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectCerrahi Tıp Bilimleri
dc.subjectPatoloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectBiyoloji ve Biyokimya
dc.subjectPATOLOJİ
dc.titleA Case Study of Intractable Diarrhea Due to Neonatal Microvillous Inclusion Disease
dc.typeMakale
dc.relation.journalFETAL AND PEDIATRIC PATHOLOGY
dc.contributor.departmentIstanbul Goztepe Training and Research Hospital , ,
dc.identifier.volume36
dc.identifier.issue4
dc.identifier.startpage340
dc.identifier.endpage343
dc.contributor.firstauthorID238838


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