Literature DB >> 27387888

Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome.

Pooja Chauhan1, Sushil Kumar Jaiswal1, Anjali Rani Lakhotia2, Amit Kumar Rai3.   

Abstract

PURPOSE: In the present study, we reported two cases of TS with mosaic ring X chromosome showing common clinical characteristics of TS like growth retardation and ovarian dysfunction. The purpose of the present study was to cytogenetically characterize both cases.
METHODS: Whole blood culture and G-banding were performed for karyotyping the cases following standard protocol. Origin of the ring chromosome and degree of mosaicism were further determined by fluorescence in situ hybridization (FISH). Breakpoints and loss of genetic material in formation of different ring X chromosomes r (X) in cases were determined with the help of cytogenetic microarray.
RESULTS: Cases 1 and 2 with ring chromosome were cytogenetically characterized as 45, X [114]/46Xr (X) (p22.11q21.32) [116] and 45, X [170]/46, Xr (X) (p22.2q21.33) [92], respectively. Sizes of these ring X chromosomes were found to be ~75 and ~95 Mb in cases 1 and 2, respectively, using visual estimation as part of cytogenetic observation. In both cases, we observed breakpoints on Xq chromosome were within relatively narrow region between Xq21.33 and Xq22.1 compared to regions in previously reported cases associated with ovarian dysgenesis.
CONCLUSIONS: Our observation agrees with the fact that despite of large heterogeneity, severity of the cases with intact X-inactive specific transcript (XIST) is dependent on degree of mosaicism and extent of Xq deletion having crucial genes involved directly or indirectly in various physiological involving ovarian cyclicity.

Entities:  

Keywords:  Cytogenetic microarray; Fluorescence in situ hybridization (FISH); Ovarian dysfunction; Ring X chromosome; Turner syndrome

Mesh:

Year:  2016        PMID: 27387888      PMCID: PMC5010817          DOI: 10.1007/s10815-016-0761-x

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


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1.  Genotype-phenotype correlation in 75 patients with small supernumerary marker chromosomes.

Authors:  Tingting Li; Haiquan Sang; Guoming Chu; Yuanyuan Zhang; Manlong Qi; Xiaoliang Liu; Wanting Cui; Yanyan Zhao
Journal:  Mol Cytogenet       Date:  2020-07-14       Impact factor: 2.009

2.  Origin of the X-chromosome influences the development and treatment outcomes of Turner syndrome.

Authors:  Ying Zhang; Yongchen Yang; Pin Li; Sheng Guo
Journal:  PeerJ       Date:  2021-12-09       Impact factor: 2.984

3.  Characterization of a rare mosaic X-ring chromosome in a patient with Turner syndrome.

Authors:  Hunjin Luo; Liu Ni; Yi-Qiong Yang; Xiao-Min Zhang; Hongping Huang; Sainan Tan; Chen Ling; Li Liang; Ling Wang; Tang Dan; Shu-Xiang Zhou; Chunliu Yang
Journal:  Mol Cytogenet       Date:  2022-03-31       Impact factor: 2.009

Review 4.  The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes.

Authors:  Peining Li; Barbara Dupont; Qiping Hu; Marco Crimi; Yiping Shen; Igor Lebedev; Thomas Liehr
Journal:  HGG Adv       Date:  2022-09-10

5.  C-banding and AgNOR-staining were still effective complementary methods to indentify chromosomal heteromorphisms and some structural abnormalities in prenatal diagnosis.

Authors:  Jian Jiang Zhu; Hong Qi; Li Rong Cai; Xiao Hui Wen; Wen Zeng; Guo Dong Tang; Yao Luo; Ran Meng; Xue Qun Mao; Shao Qin Zhang
Journal:  Mol Cytogenet       Date:  2019-09-18       Impact factor: 2.009

  5 in total

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