Incidental finding of APC deletion in a child: double trouble or double chance? - a case report

• Main Authors: Erica Rosina (Author), Berardo Rinaldi (Author), Rosamaria Silipigni (Author), Luca Bergamaschi (Author), Giovanna Gattuso (Author), Stefano Signoroni (Author), Silvana Guerneri (Author), Alessandra Carnevali (Author), Paola Giovanna Marchisio (Author), Donatella Milani (Author)
• Format: Book
• Published: BMC, 2021-02-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background 22q11.2 deletion syndrome is one of the most common genomic disorders, characterized by the variable presence of facial dysmorphisms, congenital cardiac defects, velopharyngeal insufficiency/cleft palate, thymic hypoplasia/aplasia, immunodeficiency, parathyroid hypoplasia, develo...