Prenatal Diagnosis Of Catch22 Syndrome

• Main Authors: Rana Karayalçın (Author), Serdar Ceylaner (Author), Feride İffet Şahin (Author), Şebnem Özyer (Author), Melike Doğanay (Author), Nuri Danışman (Author)
• Format: Book
• Published: Medical Network, 2010-08-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Deletions involving the long arm of chromosome 22 (22q11) are involved in various congenital heart diseases and congenital anomalies. In most cases, patients also have the features of DiGeorge Syndrome (DGS), Velocardiofacial Syndrome (VCFS), Shprintzen Syndrome, Conotruncal Anomaly Face Syndrome (C...