Incidental discovery of DMD gene deletions by chromosomal microarray analysis.
10.3760/cma.j.issn.1003-9406.2019.08.005
- Author:
Tingting SONG
1
;
Yu LI
;
Ying XU
;
Yinghui DANG
;
Shanning WAN
;
Yunyun ZHENG
;
Jianfang ZHANG
Author Information
1. Department of Obstetrics and Gynecology, the First Affiliated Hospital of Air Force Medical University, Xi'an, Shaanxi 710032, China. zhangjf@fmmu.edu.cn.
- Publication Type:Journal Article
- MeSH:
Dystrophin;
genetics;
Exons;
Female;
Fetus;
Gene Deletion;
Humans;
Incidental Findings;
Male;
Microarray Analysis;
Muscular Dystrophy, Duchenne;
genetics;
Pregnancy
- From:
Chinese Journal of Medical Genetics
2019;36(8):773-776
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To discuss the value of chromosomal microarray analysis (CMA) for the identification of DMD gene deletions during prenatal diagnosis.
METHODS:G-banded karyotyping and CMA were performed on fetuses with ultrasonographic soft markers but no family history for Duchenne/Becker muscular dystrophy (DMD/BMD). Denaturing high-performance liquid chromatograghy (DHPLC) was used to detect DMD gene mutations in umbilical cord blood and peripheral blood samples from the mothers.
RESULTS:For fetus 1, analysis of amniocytes showed a normal karyotype, while CMA detected a 119 kb deletion at Xp21.1 (32 565 489 - 32 681 461), which encompassed exons 10 to 16 of the DMD gene. The result was confirmed by DHPLC analysis. The mother was found to have loss of heterozygosity in the same region. For fetus 2, karyotyping of amniocytes also showed a normal male karyotype, while CMA detected a 254 kb deletion at Xp21.1 (32 104 604 - 32 358 874), which encompassed exons 41 to 44 of the DMD gene. The same deletion was not detected in the mother. DHPLC analysis confirmed the presence of both deletions.
CONCLUSION:Two fetuses harboring DMD gene deletions but without a family history were discovered. CMA can improve the efficiency for detecting single gene diseases caused by deletions.
