Literature DB >> 10545600

The origin of the extra Y chromosome in males with a 47,XYY karyotype.

D O Robinson1, P A Jacobs.   

Abstract

The presence of an extra Y chromosome in males is a relatively common occurrence, the 47,XYY karyotype being found in approximately 1 in 1000 male births. The error of disjunction must occur either during paternal meiosis II or as a post-zygotic mitotic error, both of which are rare events for other chromosomes. It is therefore of interest to determine when errors of Y chromosome disjunction occur. It is possible to distinguish between the different mechanisms of non-disjunction by analysing DNA polymorphisms at the distal tip of the Xp/Yp pseudoautosomal region in 47,XYY males, their parents and in some cases paternal grandparents. A cohort of 28 non-mosaic 47,XYY males was analysed. The results show that there are at least two mechanisms causing non-disjunction of the Y chromosome. In 16 of the 19 cases from which parents were available, the extra Y was generated by non-disjunction at meiosis II after a normal chiasmate meiosis I. Three cases were due to either a post-zygotic mitotic error or non-disjunction at meiosis II after a nullichiasmate meiosis I. Of the nine cases with no parental DNA available, at least four were due to meiosis II non-disjunction following a normal chiasmate meiosis I.

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Year:  1999        PMID: 10545600     DOI: 10.1093/hmg/8.12.2205

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  9 in total

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Journal:  Indian J Hum Genet       Date:  2013-07

Review 2.  Function of the sex chromosomes in mammalian fertility.

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Journal:  Cold Spring Harb Perspect Biol       Date:  2011-10-01       Impact factor: 10.005

3.  Decreased XY recombination and disturbed meiotic prophase I progression in an infertile 48, XYY, +sSMC man.

Authors:  Liu Wang; Zhipeng Xu; Furhan Iqbal; Liangwen Zhong; Yuanwei Zhang; Caiyun Wu; Guixiang Zhou; Hanwei Jiang; Ihtisham Bukhari; Howard J Cooke; Qinghua Shi
Journal:  Chromosome Res       Date:  2015-01-28       Impact factor: 5.239

4.  Oral health management of a patient with 47,XYY syndrome.

Authors:  Altaf Hussain Shah; B S Manjunatha; Naif A Bindayel; Rita Khounganian
Journal:  BMJ Case Rep       Date:  2013-12-05

5.  Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY.

Authors:  Jeannie Visootsak; John M Graham
Journal:  Dev Disabil Res Rev       Date:  2009

6.  Male infertility related to an aberrant karyotype, 47,XYY: four case reports.

Authors:  Faeza El-Dahtory; Hany M Elsheikha
Journal:  Cases J       Date:  2009-01-08

Review 7.  Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives.

Authors:  Wafa Slimani; Afef Jelloul; Ahmed Al-Rikabi; Amira Sallem; Yosra Hasni; Salma Chachia; Adel Ernez; Anouar Chaieb; Mohamed Bibi; Thomas Liehr; Ali Saad; Soumaya Mougou-Zerelli
Journal:  J Assist Reprod Genet       Date:  2020-05-12       Impact factor: 3.412

8.  Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Authors:  Nuala H Simpson; Laura Addis; William M Brandler; Vicky Slonims; Ann Clark; Jocelynne Watson; Thomas S Scerri; Elizabeth R Hennessy; Patrick F Bolton; Gina Conti-Ramsden; Benjamin P Fairfax; Julian C Knight; John Stein; Joel B Talcott; Anne O'Hare; Gillian Baird; Silvia Paracchini; Simon E Fisher; Dianne F Newbury
Journal:  Dev Med Child Neurol       Date:  2013-10-09       Impact factor: 5.449

9.  Microspherophakia in a 47, XYY Syndrome Patient: A Case Report.

Authors:  Maria Lourdes Rubalcava-Soberanis; Bani Antonio-Aguirre; Cristina Mendoza Velásquez; Andric Christopher Perez-Ortiz; Claudia Palacio-Pastrana
Journal:  Case Rep Ophthalmol       Date:  2020-01-03
  9 in total

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