Back to Authors

Zepeda-Mendoza, Cinthya J

0000-0002-0434-4965

Mayo Clinic

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

Citations 12

Molecular characterization and reclassification of a 1.18 Mbp DMD duplication following positive carrier screening for Duchenne/Becker muscular dystrophy
Zepeda‐Mendoza, Cinthya , Bontrager, Jordan E., Fisher, Camille F., McDonald, Amber , George‐Abraham, Jaya K. , Hasadsri, Linda , Zepeda-Mendoza, Cinthya J , Fisher, Camille

Clinical Case Reports | July 11, 2022 | Volume: 10 | Issue: 7 | Pages: No page available

10.1002/ccr3.6008 Get It

Abstract A 2‐month‐old male patient harboring a duplication of DMD exons 1–7 classified as pathogenic by an outside institution presented with mildly elevated creatine phosphokinase (CK); molecular breakpoint analysis by our laboratory reclassified the duplication as likely benign. To date, proband continues to develop normally with decreased CK, further supporting our reclassification.
Prenatal characterization of a novel inverted SMAD2 duplication by mate pair sequencing in a fetus with dextrocardia
Zepeda‐Mendoza, Cinthya , Essendrup, Anna, Smoley, Stephanie A., Johnson, Sarah H. , Hoppman, Nicole L., Vasmatzis, George , Jackson, Daniel L. , Kearney, Hutton M. , Zepeda-Mendoza, Cinthya J , Baughn, Linda B.

Clinical Case Reports | December 11, 2020 | Volume: 9 | Issue: 2 | Pages: 769-774

10.1002/ccr3.3608 Get It

AbstractThis case report underlines the importance of molecular characterization of genomic duplications and other structural variants in the prenatal setting to guide clinical interpretation, genetic counseling, and perinatal medical care.