Analysis of HNF1B gene variant in a fetus featuring infantile polycystic kidney disease.
10.3760/cma.j.cn511374-20210109-00024
- Author:
Yan ZHANG
1
;
Lina ZENG
;
Li LIN
;
Xian DONG
Author Information
1. Center of Prenatal Diagnosis, The Affiliated Hospital of Putian College, Putian, Fujian 351100, China. zhangyanyan840821@163.com.
- Publication Type:Journal Article
- MeSH:
Female;
Fetus;
Hepatocyte Nuclear Factor 1-beta/genetics*;
Humans;
Mutation;
Phenotype;
Polycystic Kidney, Autosomal Recessive;
Pregnancy;
Prenatal Diagnosis;
Whole Exome Sequencing
- From:
Chinese Journal of Medical Genetics
2022;39(2):205-208
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic basis for a fetus featuring infantile polycystic kidney disease (IPKD).
METHODS:Following elective abortion, fetal tissue and peripheral blood samples of its parents were collected for the extraction of genomic DNA. Whole exome sequencing was carried out to detect potential variants correlated with the phenotype.
RESULTS:The fetus was found to harbor a heterozygous c.1370C>T (p.P457L) variant of the HNF1B gene, which was unreported previously. The same variant was not detected in either parent.
CONCLUSION:The heterozygous c.1370C>T (p.P457L) variant of the HNF1B gene probably underlay the IPKD in this fetus. Above finding has enabled genetic counseling and prenatal diagnosis for the family.
