Genetic testing and prenatal diagnosis for a Chinese pedigree affected with Meckel-Gruber syndrome.
10.3760/cma.j.cn511374-20200606-00413
- Author:
Zhihui JIAO
1
;
Ganye ZHAO
;
Lina LIU
;
Yu GUO
;
Xiangdong KONG
Author Information
1. Genetics and Prenatal Diagnosis Center, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China. kongxd@263.net.
- Publication Type:Journal Article
- MeSH:
China;
Ciliary Motility Disorders;
Encephalocele/genetics*;
Female;
Genetic Testing;
Humans;
Pedigree;
Polycystic Kidney Diseases/genetics*;
Pregnancy;
Prenatal Diagnosis;
Retinitis Pigmentosa
- From:
Chinese Journal of Medical Genetics
2021;38(12):1204-1207
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To carry out genetic testing and prenatal diagnosis for a Chinese couple whom had conceived two fetuses featuring multiple malformations including polycystic kidney, polydactyly and encephalocele.
METHODS:Following elective abortion, the fetus from the second pregnancy was subjected to whole exome sequencing. Suspected pathogenic variants were verified by Sanger sequencing of the fetus and its parents.
RESULTS:The fetus was found to harbor compound heterozygous variants of the CEP290 gene, namely c.2743G>T (p.E915X) and c.2587-2A>T, which were respectively inherited from its father and mother. The same variants were not detected among 100 healthy controls nor reported previously. Bioinformatic analysis suggested both variants to be deleterious. The fetus was diagnosed with Meckel-Gruber syndrome. Prenatal diagnosis for the couple during their next pregnancy suggested that the fetus did not carry the above pathogenic variants.
CONCLUSION:The compound heterozygous variants of the CEP290 gene probably underlay the pathogenesis of Meckel-Gruber syndrome in the second fetus. Above finding has provided a basis for genetic counseling and prenatal diagnosis for the couple, and also enriched the mutational spectrum of the CEP290 gene.
