Literature DB >> 15513983

A constitutional complex chromosome rearrangement involving meiotic arrest in an azoospermic male: case report.

R Coco1, M I Rahn, P García Estanga, G Antonioli, A J Solari.   

Abstract

Complex chromosome rearrangements are rare aberrations that frequently lead to reproductive failure and that may hinder assisted reproduction. A 25-year-old azoospermic male was studied cytogenetically with synaptonemal complex analysis of spermatocytes from a testicular biopsy and fluorescence in situ hybridization (FISH) of lymphocytes. The spermatocytes showed a pentavalent plus a univalent chromosome. Cell death occurred mainly at advanced pachytene stages. The sex chromosomes were involved in the multiple, as shown by their typical axial excrescences. Two autosomal pairs, including an acrocentric chromosome (15), were also involved in the multiple. FISH allowed the definite identification of all the involved chromosomes. An inverted chromosome 12 is translocated with most of one long arm of chromosome 15, while the centromeric piece of this chromosome 15 is translocated with Yqh, forming a small marker chromosome t(15;Y). The euchromatic part of the Y chromosome is joined to the remaining piece of chromosome 12, forming a neo-Y chromosome. The patient shows azoospermia and a normal phenotype. The disruption of spermatogenesis is hypothetically due to the extent of asynaptic segments and to sex-body association during pachytene. This CCR occurred 'de novo' during paternal spermatogenesis. Meiotic analysis and FISH are valuable diagnostic tools in these cases.

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Year:  2004        PMID: 15513983     DOI: 10.1093/humrep/deh506

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  7 in total

1.  Meiotic segregation and interchromosomal effects in a rare (1:2:10) complex chromosomal rearrangement.

Authors:  Gordon Kirkpatrick; Sai Ma
Journal:  J Assist Reprod Genet       Date:  2011-11-22       Impact factor: 3.412

2.  Sequential FISH allows the determination of the segregation outcome and the presence of numerical anomalies in spermatozoa from a t(1;8;2)(q42;p21;p15) carrier.

Authors:  Anna Godo; Joan Blanco; Francesca Vidal; Mònica Parriego; Montserrat Boada; Ester Anton
Journal:  J Assist Reprod Genet       Date:  2013-08-23       Impact factor: 3.412

3.  Familial complex chromosome rearrangement (CCR) involving 5 breakpoints on chromosomes 1, 3 and 13 in a severe oligozoospermic patient.

Authors:  Lin Li; Xueyuan Heng; Wang Yun; Shuqi Zheng; Jixia Zhang; Wufang Fan
Journal:  J Assist Reprod Genet       Date:  2013-02-05       Impact factor: 3.412

4.  Complex chromosomal rearrangement involving chromosomes 1, 4 and 22 in an infertile male: case report and literature review.

Authors:  I Salahshourifar; N Shahrokhshahi; T Tavakolzadeh; Z Beheshti; H Gourabi
Journal:  J Appl Genet       Date:  2009       Impact factor: 3.240

5.  A Rare De novo Complex Chromosomal Rearrangement (CCR) Involving Four Chromosomes in An Oligo-asthenosperm Infertile Man.

Authors:  Saba Asia; Hamed Vaziri Nasab; Marjan Sabbaghian; Hamid Kalantari; Shabnam Zari Moradi; Hamid Gourabi; Anahita Mohseni Meybodi
Journal:  Cell J       Date:  2014-10-04       Impact factor: 2.479

6.  Complex Chromosomal Rearrangement Causes Male Azoospermia: A Case Report and Literature Review.

Authors:  Yi Liang; Yingjun Xie; Shu Kong; Qianying Pan; Wenjun Qiu; Ding Wang; Mengting Li; Sisi Lin; Zihang Liu; Xiaofang Sun
Journal:  Front Genet       Date:  2022-02-24       Impact factor: 4.599

7.  Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4.

Authors:  Qi Yao; Liu Wang; Bing Yao; Hongliu Gao; Weiwei Li; Xinyi Xia; Qinghua Shi; Yingxia Cui
Journal:  Mol Cytogenet       Date:  2014-07-01       Impact factor: 2.009

  7 in total

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