Literature DB >> 29198538

A Nonlethal Case of Junctional Epidermolysis Bullosa and Congenital Pyloric Atresia: Compound Heterozygosity in a Patient with a Novel Integrin Beta 4 Gene Mutation.

Lauren Ko1, Cornelia L Griggs2, Konstantinos S Mylonas3, Peter T Masiakos4, Daniela Kroshinsky1.   

Abstract

We report a case of nonfatal junctional epidermolysis bullosa and pyloric atresia in a newborn. We identified a substitution (c.914C>T) for the integrin β4 gene that has been associated with favorable outcome. A novel mutation (c.2011T>G) of unknown significance was also found in this patient who is now thriving.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ITGB4 gene mutation; junctional epidermolysis bullosa; pyloric atresia; pyloroplasty; surgery

Mesh:

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Year:  2017        PMID: 29198538     DOI: 10.1016/j.jpeds.2017.09.023

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  3 in total

Review 1.  Leading edge: emerging drug, cell, and gene therapies for junctional epidermolysis bullosa.

Authors:  Allison R Keith; Kirk Twaroski; Christen L Ebens; Jakub Tolar
Journal:  Expert Opin Biol Ther       Date:  2020-03-20       Impact factor: 4.388

2.  Case Report: Uncommon Association of ITGB4 and KRT10 Gene Mutation in a Case of Epidermolysis Bullosa With Pyloric Atresia and Aplasia Cutis Congenita.

Authors:  Melinda Matyas; Diana Miclea; Gabriela Zaharie
Journal:  Front Genet       Date:  2021-07-08       Impact factor: 4.599

Review 3.  Epidermolysis bullosa with pyloric atresia: Report of two cases in consecutive siblings

Authors:  Katherine Márquez; Diego Andrés Rodríguez; Luis Alfonso Pérez; Mauricio Duarte; Luis Augusto Zárate
Journal:  Biomedica       Date:  2021-06-29       Impact factor: 0.935

  3 in total

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