Literature DB >> 9763660

Pathogenetics of 45,X/46,XY gonadal mosaicism.

K S Reddy1, V Sulcova.   

Abstract

Five patients with 45,X/46,XY mosaicism ranging from 8% to 66% of 46, XY lymphocytes in the peripheral blood were studied. Their age when chromosome studies were performed ranged from a few days to 37 yr. The phenotypic presentations were two females with gonadal dysgenesis and Turner syndrome features (cases 1 and 2), two males with ambiguous genitalia and mixed gonadal dysgenesis (cases 3 and 4), and an infertile male with an atrophic testis (case 5). Fluorescence in situ hybridization (FISH) using dual-color X and Y probes on paraffin-embedded sections of the gonads was performed to assess mosaicism. A mosaic cell line with a Y chromosome was present in the streak ovary, dysgenetic gonad, and testis. In the mixed gonadal dysgenesis cases (cases 3 and 4), the testis had a higher percentage (greater than two fold) of XY cells than the ovary had. However, the highest ratio of cells with a Y chromosome was in the atrophic testis of the infertile male (case 5). The distribution of mosaic clones in the different gonadal cell types was examined. Both females (cases 1 and 2) with dysgenetic gonads had scant ovarian stroma and nests of Leydig or hilus cells. In FISH studies, the coelomic epithelial cells were predominantly 46,XY; in comparison, the Leydig and hilus cells had a lower percentage and the ovarian stroma the least number of cells with a Y signal. A mixed gonadal dysgenesis case (case 3) possessed a right testis with an XY complement in approximately 21% of Sertoli cells and approximately 14% of Leydig cells. The infertile male had an atrophic testis with interstitial hyperplasia (case 5). His testis contained Sertoli cells but no evidence of spermatogenesis. FISH detected a Y signal in about 50-60% of the Sertoli and Leydig cells.

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Year:  1998        PMID: 9763660     DOI: 10.1159/000015064

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  5 in total

1.  Short stature in children with an apparently normal male phenotype can be caused by 45,X/46,XY mosaicism and is susceptible to growth hormone treatment.

Authors:  Annette Richter-Unruh; Sabine Knauer-Fischer; Stefan Kaspers; Beate Albrecht; Gabriele Gillessen-Kaesbach; Berthold P Hauffa
Journal:  Eur J Pediatr       Date:  2004-02-18       Impact factor: 3.183

2.  SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype.

Authors:  Remko Hersmus; Hans Stoop; Erin Turbitt; J Wolter Oosterhuis; Stenvert Ls Drop; Andrew H Sinclair; Stefan J White; Leendert Hj Looijenga
Journal:  BMC Med Genet       Date:  2012-11-16       Impact factor: 2.103

3.  Startling mosaicism of the Y-chromosome and tandem duplication of the SRY and DAZ genes in patients with Turner Syndrome.

Authors:  Sanjay Premi; Jyoti Srivastava; Ganesan Panneer; Sher Ali
Journal:  PLoS One       Date:  2008-11-24       Impact factor: 3.240

4.  A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome.

Authors:  Noor Shafina Mohd Nor; Muhammad Yazid Jalaludin
Journal:  Int J Pediatr Endocrinol       Date:  2016-06-02

Review 5.  The Role of Number of Copies, Structure, Behavior and Copy Number Variations (CNV) of the Y Chromosome in Male Infertility.

Authors:  Fabrizio Signore; Caterina Gulìa; Raffaella Votino; Vincenzo De Leo; Simona Zaami; Lorenza Putignani; Silvia Gigli; Edoardo Santini; Luca Bertacca; Alessandro Porrello; Roberto Piergentili
Journal:  Genes (Basel)       Date:  2019-12-29       Impact factor: 4.096

  5 in total

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