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Case Report: Rothmund-Thomson syndrome type 2 in Ecuador: clinical and molecular insights into a recurrent RECQL4 variant

  • Martina Isabella Armas Samaniego
  • , Mateo Briones Vasquez
  • , Mel Mariño Zambrano
  • , Vanessa I. Romero*
  • , Karen Melo
  • , Juan Carlos Pozo-Palacios
  • *Autor correspondiente de este trabajo
  • Universidad San Francisco de Quito
  • Hospital Carlos Andrade Marin
  • University of Cuenca

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

Resumen

This case report presents two Ecuadorian patients with Rothmund-Thomson syndrome type 2 (RTS2), an autosomal recessive disorder, who share a RECQL4 variant previously identified in another Ecuadorian patient, supporting the recurrent presence of this variant in the Ecuador population. Additionally, in the Case 2 patient with a suspected compound heterozygosity, a second pathogenic variant was identified that had not been previously reported in Ecuador. These findings underscore the importance of molecular diagnosis for accurate classification of RTS2, informed risk assessment, and improved clinical care, particularly in underrepresented populations.

Idioma originalInglés
Número de artículo1695356
PublicaciónFrontiers in Pediatrics
Volumen14
DOI
EstadoPublicada - 2026

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