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p.Cys223Tyr mutation causing Crigler-Najjar syndrome type II.
Qing-Fang Xiong1, Hui Zhou1, Yong-Feng Yang1
1Department of Liver Disease, The Second Hospital of Nanjing Nanjing University of Chinese Medicine Nanjing China.
Crigler-Najjar syndrome type II is a rare genetic disorder affecting bilirubin metabolism. Early diagnosis through genetic testing and clinical evaluation is crucial for managing this condition and providing genetic counseling.
Area of Science:
- Genetics
- Biochemistry
- Pediatrics
Background:
- Crigler-Najjar syndrome (CNs) is a rare inherited disorder characterized by unconjugated hyperbilirubinemia.
- It results from mutations in the UGT1A1 gene, which encodes the enzyme UDP-glucuronosyltransferase 1A1 responsible for bilirubin conjugation.
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