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

Toshinobu IfukuSayo SuzukiYusaku NagatomoRyohei YokoyamaYoshiko YamamuraKeigo Nakatani
Published in: BMC pediatrics (2022)
As the blood flow of CPSS bypasses the liver, the levels of galactose, bile acids, and ammonia in the systemic veins can increase. Some patients with CPSS have CHD, and these toxic substances may cause liver and lung lesions as well as portosystemic encephalopathy (PSE). Several genetic chromosomal abnormalities, including 22qDS, and CPSS have similar symptoms, and neurodevelopmental abnormalities, particularly those caused by PSE, may be difficult to diagnose. Blood tests, such as newborn screening, and abdominal imaging are useful in the early diagnosis of CPSS.
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