Literature DB >> 16879197

Phenotypic variability in isodicentric Y patients: study of nine cases.

M DesGroseilliers1, M Beaulieu Bergeron, P Brochu, E Lemyre, N Lemieux.   

Abstract

Isodicentric chromosomes are the most commonly reported aberrations of the human Y chromosome. As they are unstable during cell division and can generate various types of cell lines, most reported patients are chromosomal mosaics, generally including a 45,X cell line. Phenotypes depend on the location of the breakpoints as well as on the proportion of each cell line and vary from male to abnormal female or individual with ambiguous genitalia. Although phenotypic variability is known to also depend on the degree of mosaicism in the various tissues, gonads are rarely studied. We report nine cases of isodicentric Y chromosomes studied by conventional and molecular cytogenetic: three males, five females, and one individual with sexual ambiguity. Two males had a non-mosaic karyotype, while the third male was a mosaic with a predominant 46,XY cell line. Three of the females had a major 45,X cell line, while the last two females and the patient with ambiguous genitalia had a major 46,X,idic(Y) cell line. Analyses of gonadal tissues from the individual with sexual ambiguity and of three of the five female patients gave results concordant with their phenotype, allowing us to better understand the sexual differentiation of these patients.

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Year:  2006        PMID: 16879197     DOI: 10.1111/j.1399-0004.2006.00654.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  11 in total

1.  Isodicentric Yq mosaicism presenting as infertility and maturation arrest without altered SRY and AZF regions.

Authors:  Kyle J Lehmann; Jason R Kovac; Jie Xu; Marc Anthony Fischer
Journal:  J Assist Reprod Genet       Date:  2012-06-24       Impact factor: 3.412

2.  A non-mosaic isodicentric Y chromosome resulting from breakage and fusion at the Yq pseudo-autosomal region in a fetus.

Authors:  Long-Ching Kuan; Mei-Tsz Su; Ming Chen; Pao-Lin Kuo; Tsung-Cheng Kuo
Journal:  J Assist Reprod Genet       Date:  2013-10-25       Impact factor: 3.412

3.  Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression.

Authors:  Judith L Ross; Luke Bloy; Timothy P L Roberts; Judith Miller; Chao Xing; Lawrence A Silverman; Andrew R Zinn
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2019-06-03       Impact factor: 3.568

4.  FISH and array CGH characterization of de novo derivative Y chromosome (Yq duplication and partial Yp deletion) in an azoospermic male.

Authors:  Ewa Wiland; Alexander N Yatsenko; Archana Kishore; Halina Stanczak; Agata Zdarta; Marcin Ligaj; Marta Olszewska; Jan Karol Wolski; Maciej Kurpisz
Journal:  Reprod Biomed Online       Date:  2015-05-07       Impact factor: 3.828

5.  Isodicentric Y mosaicism involving a 46, XX cell line: Implications for management.

Authors:  Lauren E Hipp; Lauren H Mohnach; Sainan Wei; Inas H Thomas; Maha E Elhassan; David E Sandberg; Elisabeth H Quint; Catherine E Keegan
Journal:  Am J Med Genet A       Date:  2015-09-26       Impact factor: 2.802

6.  A case of mosaic Klinefelter syndrome associated with isodicentric Yp.

Authors:  Hiroshi Tomomasa; Kazue Ogawa; Joji Nagasawa; Satoshi Satoh; Hiroshi Muramatsu; Tetsuro Iiyama; Hiroshi Okada
Journal:  Reprod Med Biol       Date:  2008-12-07

7.  Interstitial 4q Deletion and Isodicentric Y-Chromosome in a Patient with Dysmorphic Features.

Authors:  T I Mancini; M M Oliveira; A R N Dutra; A B A Perez; R M Minillo; S S Takeno; M I Melaragno
Journal:  Mol Syndromol       Date:  2012-05-11

8.  Diversity of sex chromosome abnormalities in a cohort of 95 Indonesian patients with monosomy X.

Authors:  Nanis S Marzuki; Helena W Anggaratri; Lita P Suciati; Debby D Ambarwati; Chrysantine Paramayuda; Hannie Kartapradja; Aman B Pulungan; Alida Harahap
Journal:  Mol Cytogenet       Date:  2011-10-12       Impact factor: 2.009

9.  Three patients with 46,X,inv(Y)(p11.2q11.2)pat/45,X and their pedigree analysis.

Authors:  Yunchun Chen; Yuni Xu; Xiaoqiang Cao; Chunqiao Zheng; Liying Lin; Zhongyuan Zhu; Jiandong Hu
Journal:  Ann Hum Genet       Date:  2020-03-12       Impact factor: 1.670

10.  A de novo derivative Y chromosome (partial Yq deletion and partial duplication of Yp and Yq) in a female with disorders of sex development.

Authors:  Qing-Song Liu; Xing-Chun Zhu; Qiang Ma; Cheng He; Jian-Lan Shao
Journal:  Clin Case Rep       Date:  2018-07-07
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