Myelomeningocele in a newborn with VACTERL association
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.
Authors
- Nicolle Correa (ORCID: https://orcid.org/0000-0002-0527-0806)
- Marjory Banda (ORCID: https://orcid.org/0009-0002-4694-4405)
- Gustavo Giraldo (ORCID: https://orcid.org/0000-0002-9367-9387)
- M. Luz Ramos (ORCID: https://orcid.org/0009-0007-1917-2362)
Institutions
- Universidad Pontificia Bolivariana (CO)
- Hospital Pablo Tobon Uribe (CO)
Publication Details
- Journal
- Archivos Argentinos de Pediatria
- Published
- 2025-11-04
- DOI
- https://doi.org/10.5546/aap.2025-10782.eng
- Primary Topic
- Esophageal and GI Pathology
- Type
- article
- Field-Weighted Citation Impact
- 0.00