Bilateral Peters' anomaly, aniridia and Wilms tumour (WAGR syndrome) in monozygotic twins.
Sebastião CronembergerAnna L B AlbuquerqueAna Cristina Simões E SilvaJovita Lane Soares Santos ZaniniAlexandre Higino Gonçalves da SilvaLuciana F BarbosaFrancine da Cunha RubiãoFelipe L de LimaRossana Fonseca CasimiroMárcio Placedino MartinsAlberto Diniz-FilhoLuciana Bastos-RodriguesEitan FriedmanLuiz Armando de MarcoPublished in: Acta paediatrica (Oslo, Norway : 1992) (2024)
WAGR syndrome is a rare contiguous gene deletion syndrome with a greater risk of developing Wilms tumour associated with Peters' anomaly and congenital aniridia. However, co-occurrence of both anomalies was rarely reported in twins, and never in both eyes of monozygotic twins. Here, we report the bilateral association of Peters' anomaly and congenital aniridia in monozygotic twins with WAGR syndrome.