Literature DB >> 19193986

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

I Salahshourifar1, N Shahrokhshahi, T Tavakolzadeh, Z Beheshti, H Gourabi.   

Abstract

Here we describe a rare case of an apparently balanced karyotype of 46, XY, t(1;22;4)(p22.3;q11.1;q31.1) in a infertile male with oligoastenoteratozoospermia (OAT). He was the second patient with complex chromosomal rearrangement (CCR) referred to our center because of infertility. We also review reports on 24 males carrying CCRs with spermatogenesis failure or a malformed child, to provide information on the reproductive outcome of male CCR carriers.

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Year:  2009        PMID： 19193986     DOI： 10.1007/BF03195655

Source DB:  PubMed          Journal:  J Appl Genet        ISSN： 1234-1983            Impact factor:   3.240


  24 in total

1.  Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.

Authors:  B Röthlisberger; D Kotzot; L Brecevic; M Koehler; D Balmer; F Binkert; A Schinzel
Journal:  Eur J Hum Genet       Date:  1999-12       Impact factor: 4.246

2.  An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.

Authors:  Iris Bartels; Heike Starke; Loukas Argyriou; Simone M Sauter; Barbara Zoll; Thomas Liehr
Journal:  Eur J Med Genet       Date:  2006-11-10       Impact factor: 2.708

3.  Preimplantation genetic diagnosis for complex chromosome rearrangements.

Authors:  T Escudero; A Estop; J Fischer; S Munne
Journal:  Am J Med Genet A       Date:  2008-07-01       Impact factor: 2.802

4.  Reproductive risks for carriers of complex chromosome rearrangements: analysis of 25 families.

Authors:  J L Gorski; M L Kistenmacher; H H Punnett; E H Zackai; B S Emanuel
Journal:  Am J Med Genet       Date:  1988-02

5.  Pachytene analysis in males heterozygous for a familial translocation (9;12;13) (q22; q22; q32) ascertained through a child with partial trisomy 9.

Authors:  R Johannisson; U Löhrs; E Passarge
Journal:  Cytogenet Cell Genet       Date:  1988

6.  Familial complex autosomal translocations involving chromosomes 7, 8, and 9 exhibiting male and female transmission with segregation and recombination.

Authors:  S Walker; P J Howard; D Hunter
Journal:  J Med Genet       Date:  1985-12       Impact factor: 6.318

7.  A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility.

Authors:  A Joseph; I M Thomas
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318

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

Authors:  J P Siffroi; B Benzacken; B Straub; C Le Bourhis; M O North; G Curotti; V Bellec; S Alvarez; J P Dadoune
Journal:  Mol Hum Reprod       Date:  1997-10       Impact factor: 4.025

9.  Constitutional complex chromosomal rearrangements in azoospermic men--case report and literature review.

Authors:  I-Wen Lee; Mei-Tsz Su; Chao-Chin Hsu; Ying-Hui Lin; Pei-Yi Chen; Pao-Lin Kuo
Journal:  Urology       Date:  2006-12       Impact factor: 2.649

10.  Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.

Authors:  Houda Karmous-Benailly; Fabienne Giuliano; Christophe Massol; Catherine Bloch; Dominique De Ricaud; Jean-Claude Lambert; Serge Perelman
Journal:  Eur J Med Genet       Date:  2006-02-10       Impact factor: 2.708
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  5 in total

1.  Azoospermia related to a unique karyotype: 45,XY,-13,-19,+der(19)t(13;19)(q12;p13).

Authors:  Chao Fu; Xin Yun; Yuan Dong; Bai-Yan Wu; Rong-Rong Han; Rui-Zhi Liu
Journal:  J Appl Genet       Date:  2011-03-08       Impact factor: 3.240

2.  A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.

Authors:  Natalia Trpchevska; Ivanka Dimova; Tatyana Arabadji; Tanya Milachich; Svetlana Angelova; Magdalena Dimitrova; Mariela Hristova-Savova; Petya Andreeva; Tania Timeva; Atanas Shterev
Journal:  J Assist Reprod Genet       Date:  2017-02-24       Impact factor: 3.412

3.  Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism.

Authors:  Ruth Mikelsaar; Jelena Lissitsina; Oliver Bartsch
Journal:  J Appl Genet       Date:  2011-04-05       Impact factor: 3.240

4.  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

5.  Identification of a familial complex chromosomal rearrangement by optical genome mapping.

Authors:  Yang Yang; Wang Hao
Journal:  Mol Cytogenet       Date:  2022-09-21       Impact factor: 1.904
  5 in total

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