Copyright
©The Author(s) 2024.
World J Clin Pediatr. Dec 9, 2024; 13(4): 98462
Published online Dec 9, 2024. doi: 10.5409/wjcp.v13.i4.98462
Published online Dec 9, 2024. doi: 10.5409/wjcp.v13.i4.98462
Hyperbilirubinemia | |||
Mutation | Total serum bilirubin ≥ 342 µmol/L | Total serum bilirubin < 342 μmol/L | P value |
Uridine 5'-diphospho-glucuronosyltransferase 1A1 | |||
G/A | 32 | 11 | 0.32 |
C/T | 4 | 3 | |
T/G | 1 | 1 | |
Na+/taurocholate cotransporting polypeptide Ntcp | |||
C/T | 6 | 7 | NA |
Heterozygous 851del4 mutation | |||
C.852_855delTATG | 2 | 3 | 0.57 |
C.1638_1660dup | 0 | 1 | |
G/A | 0 | 1 | |
Adenosine triphosphatase 7B | |||
G/T | 1 | 0 | 0.26 |
A/C | 1 | 0 | |
G/A | 0 | 1 | |
C/T | 0 | 1 | |
Glucose-6-phosphate dehydrogenase | |||
G/T | 1 | 2 | 0.32 |
G/A | 1 | 0 | |
A/G | 0 | 1 |
- Citation: You JY, Xiong LY, Wu MF, Fan JS, Fu QH, Qiu MH. Genetic variation features of neonatal hyperbilirubinemia caused by inherited diseases. World J Clin Pediatr 2024; 13(4): 98462
- URL: https://www.wjgnet.com/2219-2808/full/v13/i4/98462.htm
- DOI: https://dx.doi.org/10.5409/wjcp.v13.i4.98462