Phenotypic analysis and variant identification of a fetus with Joubert syndrome 17.
10.3760/cma.j.cn511374-20200716-00520
- Author:
Yan ZHAO
1
;
Yanhui ZHAO
;
Yuan LYU
;
Hong PANG
Author Information
1. Department of Genetics, Shenyang Women and Children's Hospital, Shenyang, Liaoning 110011, China. panghong_yc@126.com.
- Publication Type:Journal Article
- MeSH:
Abnormalities, Multiple/genetics*;
Cerebellum/diagnostic imaging*;
Eye Abnormalities/genetics*;
Female;
Fetus;
Humans;
Kidney Diseases, Cystic;
Mutation;
Phenotype;
Pregnancy;
Retina/abnormalities*
- From:
Chinese Journal of Medical Genetics
2021;38(9):841-844
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To analyze the phenotype and genetic variant of a fetus with dysplasia of cerebellar vermis.
METHODS:Gestational status and family history of the gravida was taken in combination with the imaging results of the fetus. Following elected abortion, fetal tissue and peripheral blood samples of the couple were collected for the extraction of genome DNA. Whole exome sequencing was carried out to screen potential variant associated with the phenotype of the proband. Specific PCR primers were designed to verify the results by Sanger sequencing.
RESULTS:Prenatal ultrasound revealed that the fetal vermis cerebellum was poorly developed, which was similar to the previous pregnancy. Whole exome sequencing revealed that the fetus has carried compound heterozygous variants of the CPLANE1 gene, namely c.7978C>T and c.7169delT, which were respectively inherited from the husband and wife.
CONCLUSION:The c.7978C>T and c.7169delT compound heterozygous variants of the CPLANE1 gene probably underlay the dysplasia of cerebellar vermis in the fetus, which has provided a basis for genetic counseling and prenatal diagnosis.
