Congenital portosystemic venous shunt associated with 22q11.2 deletion syndrome: a case report

• Main Authors: Toshinobu Ifuku (Author), Sayo Suzuki (Author), Yusaku Nagatomo (Author), Ryohei Yokoyama (Author), Yoshiko Yamamura (Author), Keigo Nakatani (Author)
• Format: Book
• Published: BMC, 2022-06-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background 22q11.2 deletion syndrome (22qDS) is the most common chromosomal microdeletion syndrome and is associated with a high rate of congenital heart disease (CHD) and neurodevelopmental abnormalities. Congenital portosystemic venous shunts (CPSS) are rare developmental abnormalities of...