22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects

• Main Authors: Carolina Putotto (Author), Flaminia Pugnaloni (Author), Marta Unolt (Author), Stella Maiolo (Author), Matteo Trezzi (Author), Maria Cristina Digilio (Author), Annapaola Cirillo (Author), Giuseppe Limongelli (Author), Bruno Marino (Author), Giulio Calcagni (Author), Paolo Versacci (Author)
• Format: Book
• Published: MDPI AG, 2022-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Congenital heart diseases represent one of the hallmarks of 22q11.2 deletion syndrome. In particular, conotruncal heart defects are the most frequent cardiac malformations and are often associated with other specific additional cardiovascular anomalies. These findings, together with extracardiac man...