Literature DB >> 28842815

Congenital Fatal Diarrhea in Newborns.

Swapna Lingaldinna1, Mangala Bharathi Sundaram2, C N Kamalarathnam1, Sumathi Bavanandam3.   

Abstract

Microvillus inclusion disease is a rare autosomal recessive disorder of intestinal epithelium causing intractable secretary diarrhea in the first two months of life and about 140 cases have been reported worldwide till now. Here authors report 2 cases of Microvillus inclusion disease (MVID) diagnosed in neonates by electron microscopy study of small intestinal biopsy.

Entities:  

Keywords:  Microvillus inclusion disease; Neonatal diarrhea; Small bowel biopsy

Mesh：

Year:  2017        PMID： 28842815     DOI： 10.1007/s12098-017-2414-1

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


  6 in total

1.  Treatment of microvillus inclusion disease by intestinal transplantation.

Authors:  S K Bunn; S V Beath; P J McKeirnan; D A Kelly; J A Buckles; D Mirza; A D Mayer; J D de Goyet
Journal:  J Pediatr Gastroenterol Nutr       Date:  2000-08       Impact factor: 2.839

Review 2.  An overview and online registry of microvillus inclusion disease patients and their MYO5B mutations.

Authors:  K Joeri van der Velde; Herschel S Dhekne; Morris A Swertz; Serena Sirigu; Virginie Ropars; Petra C Vinke; Trebor Rengaw; Peter C van den Akker; Edmond H H M Rings; Anne Houdusse; Sven C D van Ijzendoorn
Journal:  Hum Mutat       Date:  2013-10-16       Impact factor: 4.878

3.  Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy.

Authors:  G P Davidson; E Cutz; J R Hamilton; D G Gall
Journal:  Gastroenterology       Date:  1978-11       Impact factor: 22.682

4.  Villin immunohistochemistry is a reliable method for diagnosing microvillus inclusion disease.

Authors:  Nick M Shillingford; Monica L Calicchio; Lisa A Teot; Theonia Boyd; Kyle C Kurek; Jeffrey D Goldsmith; Athos Bousvaros; Antonio R Perez-Atayde; Harry P W Kozakewich
Journal:  Am J Surg Pathol       Date:  2015-02       Impact factor: 6.394

5.  MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity.

Authors:  Thomas Müller; Michael W Hess; Natalia Schiefermeier; Kristian Pfaller; Hannes L Ebner; Peter Heinz-Erian; Hannes Ponstingl; Joachim Partsch; Barbara Röllinghoff; Henrik Köhler; Thomas Berger; Henning Lenhartz; Barbara Schlenck; Roderick J Houwen; Christopher J Taylor; Heinz Zoller; Silvia Lechner; Olivier Goulet; Gerd Utermann; Frank M Ruemmele; Lukas A Huber; Andreas R Janecke
Journal:  Nat Genet       Date:  2008-08-24       Impact factor: 38.330

Review 6.  Microvillous inclusion disease (microvillous atrophy).

Authors:  Frank M Ruemmele; Jacques Schmitz; Olivier Goulet
Journal:  Orphanet J Rare Dis       Date:  2006-06-26       Impact factor: 4.123
  6 in total

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