VACTERL Association in a Male Infant with an Additional Genomic Segment on Chromosome 17p

Authors

  • Samornmas Kanngurn Department of Pathology, Faculty of Medicine Siriraj Hospital, Mahidol University
  • Rathapol Suebsinsatchawong Department of Pathology, Faculty of Medicine Siriraj Hospital, Mahidol University
  • Pornprot Limprasert Department of Pathology, Faculty of Medicine Siriraj Hospital, Mahidol University

Keywords:

VACTERL, VATER, add (17), 17p , chromosome

Abstract

The case of a term Thai male infant with VACTERL anomalies including imperforate anus, atrial septal defect, tracheo-esophageal (TE) fistula, and horseshoe kidney with bilateral hydronephrosis whose chromosome study revealed an additional genomic segment of unknown origin on the short arm of chromosome 17 is reported. The karyotype is described as 46, XY, add (17) (p13), which has never been previously reported in VACTERL association.

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Published

31-07-2020

How to Cite

Kanngurn, S. ., Suebsinsatchawong, R. ., & Limprasert, P. . (2020). VACTERL Association in a Male Infant with an Additional Genomic Segment on Chromosome 17p. Siriraj Medical Journal, 64(6), 196–198. Retrieved from https://he02.tci-thaijo.org/index.php/sirirajmedj/article/view/244197

Issue

Vol. 64 No. 6 (2012): Nov-Dec

Section

Case Report

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