Literature DB >> 14676590

Neonatal enteropathies: defining the causes of protracted diarrhea of infancy.

Philip M Sherman1, David J Mitchell, Ernest Cutz.   

Abstract

The underlying causes of chronic diarrhea beginning early in life are increasingly well defined. Infectious and post-infectious enteropathies and food sensitive/allergic enteropathy account for the majority of cases. Recent attention has focused on characterizing defined entities, which cause protracted diarrhea in infants and young children. Disorders of intestinal ion transport usually present at birth following a pregnancy complicated by polyhydramnios. Intestinal mucosal biopsies show normal architect with intact villus-crypt axis. Neonatal enteropathies, by contrast, are characterized by blunting of the villi. These include microvillus inclusion disease, tufting enteropathy, autoimmune enteropathy and IPEX syndrome - and it is these conditions that are the subject of the current review.

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Year:  2004        PMID: 14676590     DOI: 10.1097/00005176-200401000-00007

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  33 in total

1.  Intractable diarrhoea of infancy caused by neutrophil specific granule deficiency and cured by stem cell transplantation.

Authors:  R F Wynn; M Sood; K Theilgaard-Mönch; C J Jones; A F Gombart; M Gharib; H P Koeffler; N Borregaard; P D Arkwright
Journal:  Gut       Date:  2006-02       Impact factor: 23.059

Review 2.  Newcomers in paediatric GI pathology: childhood enteropathies including very early onset monogenic IBD.

Authors:  Arzu Ensari; Judith Kelsen; Pierre Russo
Journal:  Virchows Arch       Date:  2017-07-17       Impact factor: 4.064

Review 3.  Recent progress in congenital diarrheal disorders.

Authors:  Roberto Berni Canani; Gianluca Terrin
Journal:  Curr Gastroenterol Rep       Date:  2011-06

4.  An 11-month-old boy with chronic diarrhea, failure to thrive, and hepatomegaly.

Authors:  Steven Liu; Jonathan E Markowitz
Journal:  MedGenMed       Date:  2007-09-12

5.  Multiple hepatic adenomas in a child with microvillus inclusion disease.

Authors:  Jennifer C Burgis; C Allan Pratt; John P T Higgins; John A Kerner
Journal:  Dig Dis Sci       Date:  2013-03-24       Impact factor: 3.199

6.  Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease.

Authors:  Agata M Szperl; Magdalena R Golachowska; Marcel Bruinenberg; Rytis Prekeris; Andy-Mark W H Thunnissen; Arend Karrenbeld; Gerard Dijkstra; Dick Hoekstra; David Mercer; Janusz Ksiazyk; Cisca Wijmenga; Martin C Wapenaar; Edmond H H M Rings; Sven C D van IJzendoorn
Journal:  J Pediatr Gastroenterol Nutr       Date:  2011-03       Impact factor: 2.839

7.  Functional consequences of EpCam mutation in mice and men.

Authors:  James L Mueller; Matthew D McGeough; Carla A Peña; Mamata Sivagnanam
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2013-12-12       Impact factor: 4.052

Review 8.  Autoimmune Enteropathy: An Updated Review with Special Focus on Stem Cell Transplant Therapy.

Authors:  Zunirah Ahmed; Aamer Imdad; James A Connelly; Sari Acra
Journal:  Dig Dis Sci       Date:  2018-11-10       Impact factor: 3.199

9.  Tufting Enteropathy with EpCAM Mutations in Two Siblings.

Authors:  Jae Sung Ko; Jeong Kee Seo; Jeong Ok Shim; Sol Ha Hwang; Heae Surng Park; Gyeong Hoon Kang
Journal:  Gut Liver       Date:  2010-09-24       Impact factor: 4.519

10.  Identification of EpCAM as the gene for congenital tufting enteropathy.

Authors:  Mamata Sivagnanam; James L Mueller; Hane Lee; Zugen Chen; Stanley F Nelson; Dan Turner; Stanley H Zlotkin; Paul B Pencharz; Bo-Yee Ngan; Ondrej Libiger; Nicholas J Schork; Joel E Lavine; Sharon Taylor; Robert O Newbury; Richard D Kolodner; Hal M Hoffman
Journal:  Gastroenterology       Date:  2008-05-15       Impact factor: 22.682

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