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VATER/VACTERL association and caudal regression with Xq25-q27.3 microdeletion: A case report

  • Surasak Puvabanditsin
  • , James Van Gurp
  • , Melissa February
  • , Marwa Khalil
  • , Julia Mayne
  • , Jennifer Ai Mcconnell
  • , Rajeev Mehta
  • Rutgers - The State University of New Jersey, New Brunswick

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

We report a term female neonate with vertebral anomalies, anal and urethral atresia, esophageal atresia with tracheoesophageal fistula (TEF), renal agenesis, pulmonary hypoplasia, genital and sacral appendages, and a single umbilical artery. Genetic studies revealed a 20.91 Mb interstitial deletion of the long arm of X chromosome: Xq25-q27.3. This is a new case of VATER/VACTERL association with Xq25 microdeletion.

Original languageEnglish
Pages (from-to)133-141
Number of pages9
JournalFetal and Pediatric Pathology
Volume35
Issue number2
DOIs
StatePublished - 3 Mar 2016

Keywords

  • congenital anomalies
  • neonate
  • VATER/VACTERL association
  • Xq25-q27.3 deletion

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