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X-linked CNV and skewed X-chromosome inactivation

https://doi.org/10.25557/2073-7998.2020.03.19-21

Abstract

A skewed X-chromosome inactivation can be a consequence and a marker of impaired cell proliferation in the presence of copy number variations (CNV) on the X chromosome. X-linked CNVs are detected in women with miscarriages and a skewed X-chromosome inactivation (with a frequency of 33.3%), as well as in patients with intellectual disability and skewed X-chromosome inactivation in their mothers (with a frequency of 40%).

About the Authors

E. A. Fonova
Research Institute of Medical Genetics, Tomsk NRMC
Russian Federation


E. N. Tolmacheva
Research Institute of Medical Genetics, Tomsk NRMC
Russian Federation


A. A. Kashevarova
Research Institute of Medical Genetics, Tomsk NRMC
Russian Federation


M. E. Lopatkina
Research Institute of Medical Genetics, Tomsk NRMC
Russian Federation


K. A. Pavlova
Siberian State Medical University
Russian Federation


I. N. Lebedev
Research Institute of Medical Genetics, Tomsk NRMC
Russian Federation


Review

For citations:


Fonova E.A., Tolmacheva E.N., Kashevarova A.A., Lopatkina M.E., Pavlova K.A., Lebedev I.N. X-linked CNV and skewed X-chromosome inactivation. Medical Genetics. 2020;19(3):19-21. (In Russ.) https://doi.org/10.25557/2073-7998.2020.03.19-21

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ISSN 2073-7998 (Print)