Literature DB >> 12891520

Esophageal atresia and tracheo-esophageal fistula in a patient with Digeorge syndrome.

S Sebnem Kilic1, Arif Gurpinar, Tahsin Yakut, Unal Egeli, Hasan Dogruyol.   

Abstract

DiGeorge Syndrome (DGS) is a congenital disorder that affects the thymus, parathyroid glands, and heart and brain. Thymus involvement in DGS may vary between absence/hypoplasia of thymus to various forms of reduced T cell function. TBX1 deficiency causes a number of distinct vascular and heart defects, suggesting multiple roles in cardiovascular development, specifically, formation and growth of the pharyngeal arch arteries, growth and septation of the outflow tract of the heart, interventricular septation, and conal alignment. Here the authors describe a case of DGS presenting with severe combined immunodeficiency, esophageal atresia, and tracheoesophageal fistula (TEF). DGS is an important differential diagnosis in TEF.

Entities:  

Mesh:

Year:  2003        PMID: 12891520     DOI: 10.1016/s0022-3468(03)00295-1

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  2 in total

Review 1.  Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology.

Authors:  C Shaw-Smith
Journal:  J Med Genet       Date:  2005-11-18       Impact factor: 6.318

2.  FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities.

Authors:  Tahsin Yakut; Sara Sebnem Kilic; Ergun Cil; Esra Yapici; Unal Egeli
Journal:  Pediatr Surg Int       Date:  2006-02-04       Impact factor: 1.827

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.