Rothmund-Thomson Syndrome Type II: A Pediatric Case Presentation with Genetic and Dermoscopic Findings
Loubaris Zineb, Moumna Rasha, Benzekri Laila & Meziane Mariame · Asian Journal of Pediatric Research · 2025
Background: Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive genodermatosis characterized by poikiloderma, sparse hair, skeletal anomalies, and an increased risk of malignancies, particularly osteosarcoma and skin cancers. RTS is classified into two types: Type I wit...
Open access
Research Article
10.9734/ajpr/2025/v15i6451