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Myelomeningocele in a newborn with VACTERL association

  • Mateo J. Murcia Ramos
  • , María F. Rodríguez Banda (Author undergraduate student)
  • , Natalia M. Mazo Correa
  • , Gustavo A. Giraldo Ospina

Research output: Contribution to scientific journalArticle in an indexed scientific journalpeer-review

Abstract

VACTERL association refers to the concomitant occurrence of congenital malformations such as vertebral defects, anorectal malformations, cardiac anomalies, tracheoesophageal fistula, renal anomalies, and limb defects. This case describes a newborn girl who presented with anomalies compatible with this association, such as scoliosis, sacral dysgenesis, right lower phocomelia, and multicystic renal dysplasia, also associated with myelomeningocele, which was surprising as it occurred concomitantly with the other congenital malformations. Although neural tube defects are not part of the classic criteria for VACTERL, their coexistence with the characteristic malformations of this association raises the possibility of broadening its phenotypic spectrum, encourages debate on the inclusion of new criteria to define it, and highlights the importance of considering systematic evaluation of the spinal cord in screening, aspects that have been little explored in Latin America.

Translated title of the contributionMielomeningocele en un neonato con asociación VACTERL: a propósito de un caso
Original languageEnglish
Pages (from-to)e202510782
JournalArchivos Argentinos de Pediatria
Volume124
Issue number3
DOIs
StatePublished - 1 Jun 2026

Bibliographical note

Publisher Copyright:
Sociedad Argentina de Pediatría.

Keywords

  • congenital anomalies
  • meningomyelocele
  • multicystic dysplastic kidney
  • spinal dysraphism

Types Minciencias

  • Artículos de investigación con calidad Q3

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