Bilateral Peters' anomaly, aniridia and Wilms tumour (WAGR syndrome) in monozygotic twins

Aim This study reports the bilateral association of Peters' anomaly and congenital aniridia in monozygotic twins subsequently diagnosed with Wilms tumour (WAGR syndrome). Methods Two monozygotic female twins were referred at age 2 months with bilateral corneal opacity. A diagnosis of Peters...

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Veröffentlicht in:	Acta Paediatrica 2024-06, Vol.113 (6), p.1420-1425
Hauptverfasser:	Cronemberger, Sebastião, Albuquerque, Anna L. B., Silva, Ana Cristina Simões e, Zanini, Jovita Lane Soares Santos, Silva, Alexandre Higino Gonçalves, Barbosa, Luciana F., Cunha Rubião, Francine, Lima, Felipe L., Casimiro, Rossana Fonseca, Martins, Márcio Placedino, Diniz‐Filho, Alberto, Bastos‐Rodrigues, Luciana, Friedman, Eitan, De Marco, Luiz
Format:	Artikel
Sprache:	eng
Schlagworte:	Aniridia Chromosome 11 Chromosome deletion Cornea Gene deletion monozygotic twins Peters' anomaly Tumors Twins WAGR syndrome Wilms' tumour
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