A case of Gilbert syndrome caused by gene compound heterozygous mutations / 浙江大学学报·医学版
Journal of Zhejiang University. Medical sciences
;
(6): 406-409, 2020.
Article
in Chinese
| WPRIM
| ID: wpr-828502
ABSTRACT
A case of Gilbert syndrome (GS) with a heterozygous mutation in the gene is reported. The patient had no symptoms except for recurrent sclera icterus since childhood. Laboratory examinations revealed an elevated unconjugated bilirubin. Biliary obstruction, hemolysis and other diseases that might cause jaundice were excluded. *28 and c.211G>A heterozygous mutations in gene were found, which may be another type of mutation causing GS in Chinese population.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Bilirubin
/
Glucuronosyltransferase
/
Asian People
/
Genetics
/
Gilbert Disease
/
Heterozygote
/
Mutation
Limits:
Humans
Language:
Chinese
Journal:
Journal of Zhejiang University. Medical sciences
Year:
2020
Type:
Article
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