Analysis of a pedigree affected with HSAS syndrome due to a noval variant of L1CAM gene.
10.3760/cma.j.cn511374-20200113-00024
- Author:
Zhidan HONG
1
;
Ling MA
;
Yanhong MAO
Author Information
1. Reproductive Medicine Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, China. 810323923@qq.com.
- Publication Type:Journal Article
- MeSH:
Adult;
Female;
Heterozygote;
Humans;
Hydrocephalus/genetics*;
Male;
Mutation;
Neural Cell Adhesion Molecule L1/genetics*;
Pedigree;
Pregnancy;
Whole Exome Sequencing
- From:
Chinese Journal of Medical Genetics
2021;38(1):83-86
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic basis for a fetus with hydrocephalus.
METHODS:The fetus was found to have hydrocephalus upon ultrasonography duringthe second trimester. Following induced abortion, fetal tissue was collected for the extraction of DNA and whole exome sequencing.Sanger sequencing was used to verify the suspected variants in the family.
RESULTS:The fetus was found to harbor a hemizygous c.620A>G (p.Tyr207Cys) variant of the L1CAM gene (OMIM 308840),for which his mother and sister were heterozygous carriers. The same variant was not found in his father, uncle and grandparents.Based on the standards and guidelines of the American College of Medical Genetics and Genomics, the variant was predicted to be likely pathogenic (PM1+PM2+PP3+PP4).
CONCLUSION:The hemizygous c.620A>G (p.Tyr207Cys) variant of the L1CAM gene probably underlay the hydrocephalus in this fetus.
