Analysis and prenatal diagnosis of FMR1 gene mutations among patients with unexplained mental retardation.
10.3760/cma.j.cn511374-20200513-00344
- VernacularTitle:不明原因智力障碍患者的
FMR1基因分析及产前诊断
- Author:
Shikun LUO
1
;
Wenbin HE
;
Yi LIAO
;
Weilin TANG
;
Xiurong LI
;
Liang HU
;
Juan DU
;
Qianjun ZHANG
;
Yueqiu TAN
;
Ge LIN
;
Wen LI
Author Information
1. Institute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, Hunan 410078, China. liwen1968@csu.edu.cn.
- Publication Type:Journal Article
- MeSH:
Female;
Fragile X Mental Retardation Protein/genetics*;
Fragile X Syndrome/genetics*;
Humans;
Intellectual Disability/genetics*;
Mutation;
Pregnancy;
Prenatal Diagnosis
- From:
Chinese Journal of Medical Genetics
2021;38(5):439-445
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To analyze the (CGG)n repeats of FMR1 gene among patients with unexplained mental retardation.
METHODS:For 201 patients with unexplained mental retardation, the (CGG)n repeats of the FMR1 gene were analyzed by PCR and FragilEase
RESULTS:For the 201 patients with unexplained mental retardation, 15 were identified with full mutations of the FMR1 gene. The prevalence of fragile X syndrome (FXS) in patients with unexplained mental retardation was determined as 7.5% (15/201). Prenatal diagnosis was provided for 6 pregnant women with pre- or full mutations. Analysis revealed that women with mental retardation and full FMR1 mutations exhibited a skewed XCI pattern with primary expression of the X chromosome carrying the mutant allele.
CONCLUSION:FXS has a high incidence among patients with unexplained mental retardation. Analysis of FMR1 gene (CGG)n repeats in patients with unexplained mental retardation can facilitate genetic counseling and prenatal diagnosis for their families. FMR1 gene (CGG)n repeats screening should be recommended for patients with unexplained mental retardation.
