Case Report: Rothmund-Thomson syndrome type 2 in Ecuador: clinical and molecular insights into a recurrent RECQL4 variant
This case report presents two Ecuadorian patients with Rothmund-Thomson syndrome type 2 (RTS2), an autosomal recessive disorder, who share a <i>RECQL4</i> 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.
Authors
- Vanessa Romero (ORCID: https://orcid.org/0000-0003-3048-9081)
- Martina Isabella Armas Samaniego
- Juan Carlos Pozo-Palacios
- Karen Melo
- Mel Mariño Zambrano
- Mateo Briones Vasquez
Institutions
- University of Cuenca (EC)
- Hospital Universitario Rey Juan Carlos (ES)
- Universidad San Francisco de Quito (EC)
Publication Details
- Journal
- Frontiers in Pediatrics
- Published
- 2026-02-09
- DOI
- https://doi.org/10.3389/fped.2026.1695356
- Primary Topic
- Lysosomal Storage Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00