Literature DB >> 27614115

Esophageal atresia with tracheoesophageal fistula in a patient with 7q35-36.3 deletion including SHH gene.

Tiffany Busa1, Nicoleta Panait2, Kathia Chaumoitre3, Nicole Philip4, Chantal Missirian5.   

Abstract

Terminal 7q deletion is rarely reported in the literature. Holoprosencephaly and sacral dysgenesis are found in association with this deletion, due to haploinsufficiency of SHH and HLBX9 genes respectively. We report on a 2-year-old boy with 7q35-36.3 deletion encompassing SHH identified by oligonucleotide array comparative genomic hybridization. In addition to other frequent features, the patient presented with esophageal atresia and tracheoeosophageal fistula diagnosed at birth. This case, together with two others previously described, one presenting with esophageal atresia, the other with congenital esophageal stenosis, confirms the possible association between congenital esophageal malformations and 7q terminal deletion including SHH.
Copyright © 2016 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  7q terminal deletion; Oesophageal atresia; SHH gene; Tracheoesophageal fistula

Mesh:

Substances:

Year:  2016        PMID: 27614115     DOI: 10.1016/j.ejmg.2016.09.001

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  2 in total

Review 1.  Twin pregnancy complicated by esophageal atresia, duodenal atresia, gastric perforation, and hypoplastic left heart structures in one twin: a case report and review of the literature.

Authors:  Mohamad K Abou Chaar; Mariana L Meyers; Bethany D Tucker; Henry L Galan; Kenneth W Liechty; Timothy M Crombleholme; Ahmed I Marwan
Journal:  J Med Case Rep       Date:  2017-03-18

2.  Case Report: Congenital Brain Dysplasia, Developmental Delay and Intellectual Disability in a Patient With a 7q35-7q36.3 Deletion.

Authors:  Liang-Liang Fan; Yue Sheng; Chen-Yu Wang; Ya-Li Li; Ji-Shi Liu
Journal:  Front Genet       Date:  2021-12-01       Impact factor: 4.599

  2 in total

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