Literature DB >> 16466147

[Esophageal atresia and chromosomal abnormalities in a Mexican children population: descriptive analysis].

J F González-Zamora1, F Villegas-Alvarez.   

Abstract

INTRODUCTION: Chromosome alterations are associated with esophageal atresia (EA) in up to 11% of the cases. The morbidity and mortality index of this population is different from other EA patients. The present study was aimed to determine the characteristics of this association in a Mexican infant patient population.
MATERIAL AND METHODS: Observational, descriptive, retrospective, transversal assay including patients with AE and chromosome alterations over a 31-year period. Gestational age, admittance age, sex, type of atresia, chromosome alteration, additional malformations, treatment, evolution and death cause, were registered.
RESULTS: Seventeen patients (4.61%) out of 368 with EA were included. Chromosome 21 trisomy was detected in 12 children and 5 with 18 trisomy. One to 3 additional malformations were found in 16 patients. Fifteen children were subjected to surgical procedures for EA, and 6 for associated malformations. Fourteen children died in a 140-day follow-up period.
CONCLUSIONS: Coexistence between AE, trisomys and major malformations was characterized by multifactorial complications which determined adverse evolution in the short term.

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Year:  2005        PMID: 16466147

Source DB:  PubMed          Journal:  Cir Pediatr        ISSN: 0214-1221


  1 in total

1.  Unusual clinical history of a male infant with Edwards syndrome.

Authors:  Andrea Surányi; Tamás Bitó; György Vajda; László Kaiser; Gábor Gáspár; Márta Katona; János Szabó; Attila Pál
Journal:  Pathol Oncol Res       Date:  2008-06-25       Impact factor: 3.201

  1 in total

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