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. 2017;111(2):140-144.
doi: 10.1159/000449241. Epub 2016 Oct 19.

Long-Gap Esophageal Atresia Is a Unique Entity within the Esophageal Atresia Defect Spectrum

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Long-Gap Esophageal Atresia Is a Unique Entity within the Esophageal Atresia Defect Spectrum

Sigrid Bairdain et al. Neonatology. 2017.

Abstract

Background: Long-gap esophageal atresia (LGEA) may have clinical and syndromic presentations different from those of esophageal atresia (EA) that affects shorter segments of the esophagus (non-LGEA). This may suggest unique underlying developmental mechanisms.

Objectives: We sought to characterize clinical differences between LGEA and non-LGEA by carefully phenotyping a cohort of EA patients, and furthermore to assess molecular genetic findings in a subset of them.

Methods: This is a retrospective cohort study to systematically evaluate clinical and genetic findings in EA infants who presented at our institution over a period of 10 years (2005-2015).

Results: Two hundred twenty-nine EA patients were identified, 69 (30%) of whom had LGEA. Tracheoesophageal fistula was present in most non-LGEA patients (158 of 160) but in only 30% of LGEA patients. The VACTERL association was more commonly seen with non-LGEA compared to LGEA (70 vs. 25%; p < 0.001). Further, trisomy 21 was more common in LGEA than in non-LGEA. 25% of LGEA patients had an isolated EA diagnosis without other anomalies, compared to <1% for non-LGEA. Chromosomal microarray analysis showed copy number variations (CNV) in 4 of 39 non-LGEA patients and 0 of 3 LGEA patients. A review of the ClinGen database showed that none of those CNV have been previously described with EA.

Conclusions: LGEA represents a unique type of EA. Compared to non-LGEA, it is more likely to be an isolated defect and associated with trisomy 21. Further, it is less commonly seen with VACTERL anomalies. Our findings suggest the involvement of unique pathways that may be distinct from those causing non-LGEA.

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Conflict of interest statement

DTM is part-time Clinical Consultant and Medical Director for Claritas Genomics, Inc., a majority owned subsidiary of Boston Children’s Hospital (non-equity professional service agreement). The remaining authors have no potential conflicts of interest to disclose.

Figures

Figure 1
Figure 1
Distribution of phenotypic categories among LGEA and non-LGEA patients. Comparisons include vertebral, anorectal, conus, cardiac, TEF, renal, limbs and esophageal defects. Asterisks denote significant group differences based on Fisher’s exact test at the p < 0.01 level and daggers indicate differences between the two groups at p < 0.05.

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References

    1. Spitz L. Oesophageal atresia. Orphanet J Rare Dis. 2007;2:24. - PMC - PubMed
    1. Foker JE, Linden BC, Boyle EM, Marquardt C. Development of a true primary repair for the full spectrum of esophageal atresia. Ann Surg. 1997;226(4):533–541. - PMC - PubMed
    1. Bairdain S, Kelly DP, Tan C, Dodson B, Zurakowski D, Jennings RW, et al. High incidence of catheter-associated venous thromboembolic events in patients with long gap esophageal atresia treated with the Foker process. J Pediatr Surg. 2014;49(2):370–3. - PubMed
    1. Gross RE. The surgery of infancy and childhood. Philadelphia: Saunders; 1953.
    1. David TJ, O’Callaghan SE. Oesophageal atresia in the South West of England. J Med Genet. 1975;12(1):1–11. - PMC - PubMed

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