Literature DB >> 9395262

Assisted reproductive technology and complex chromosomal rearrangements: the limits of ICSI.

J P Siffroi1, B Benzacken, B Straub, C Le Bourhis, M O North, G Curotti, V Bellec, S Alvarez, J P Dadoune.   

Abstract

Complex chromosomal rearrangements are very rare events in the human population. According to our knowledge on the consequences of simple reciprocal translocations for male fertility, translocations involving three or more chromosomes are thought to lead to severe reproductive impairments in terms of meiotic disturbance or chromosomal imbalance of gametes. We report the case of a 48 year old man whose sperm count revealed either oligozoospermia (<10(3) spermatozoa/ml) or azoospermia. He was referred to the laboratory for in-vitro fertilization after intracytoplasmic sperm injection. Cytogenetic investigations showed a complex chromosomal rearrangement involving firstly a translocation between the short arm of chromosome 7 and the long arm of chromosome 13 and secondly a translocation between the short arm of the same chromosome 13 and the short arm of chromosome 9. Diagnosis was ascertained by fluorescence in-situ hybridization and staining of the nucleolar organizer regions. Theoretical study of the translocated chromosomes predicted a 'chain' configuration of the hexavalent at the pachytene stage of meiosis. In all, 32 modes of segregation were considered and only one resulted either in a normal or a balanced gamete karyotype. Genetic counselling and choice of appropriate artificial reproduction technique are discussed.

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Year:  1997        PMID: 9395262     DOI: 10.1093/molehr/3.10.847

Source DB:  PubMed          Journal:  Mol Hum Reprod        ISSN: 1360-9947            Impact factor:   4.025


  7 in total

1.  De novo complex chromosomal rearrangement of 46, XY, t (3; 16; 8) (p26; q13; q21.2) in a non-obstructive azoospermic male.

Authors:  Iman Salahshourifar; Mohammad Ali Sedighi Gilani; Ahmad Vosough; Tayebeh Tavakolzadeh; Masoumeh Tahsili; Zahra Mansori; Hamideh Karimi; Mehdi Totonchi; Hamid Gourabi
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

2.  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

Review 3.  Male infertility due to testicular disorders.

Authors:  Aditi Sharma; Suks Minhas; Waljit S Dhillo; Channa N Jayasena
Journal:  J Clin Endocrinol Metab       Date:  2021-01-23       Impact factor: 5.958

4.  A familial rearrangement(3;5;9) with paternal and maternal transmission leading to a duplication 3p/ deletion 5p infant.

Authors:  Horacio Rivera; María G Domínguez
Journal:  Clinics (Sao Paulo)       Date:  2012       Impact factor: 2.365

5.  Non-obstructive azoospermia and maturation arrest with complex translocation 46,XY t(9;13;14)(p22;q21.2;p13) is consistent with the Luciani-Guo hypothesis of latent aberrant autosomal regions and infertility.

Authors:  Eric Scott Sills; Joseph Jinsuk Kim; Michael A Witt; Gianpiero D Palermo
Journal:  Cell Chromosome       Date:  2005-09-14

6.  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

7.  Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding.

Authors:  Nilüfer Karadeniz; Kristin Mrasek; Anja Weise
Journal:  Mol Cytogenet       Date:  2008-08-07       Impact factor: 2.009

  7 in total

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