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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
  • Universidad San Francisco de Quito
  • Hospital Carlos Andrade Marin

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Article number1695356
JournalFrontiers in Pediatrics
Volume14
DOIs
StatePublished - 2026

Keywords

  • Ecuador
  • RECQL4
  • Rothmund-Thomson syndrome type 2
  • clinical genetics
  • molecular diagnosis
  • rare diseases

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