Literature DB >> 7567329

Sex chromosome tetrasomy and pentasomy.

M G Linden1, B G Bender, A Robinson.   

Abstract

Sex chromosome abnormalities occur in at least 1 in 400 births and include the well-described 47,XXX, 47,XXY, 47,XYY, and 45,X karyotypes. The addition of more than one extra X or Y chromosome occurs rarely, and little information is available in the medical literature. Individual case reports make up most of this body of knowledge, and all are based on subjects who identified themselves postnatally. Many were ascertained through screenings of institutions and hospitals; thus, there is no unbiased information on the natural history of poly X and Y karyotypes. A direct relationship between the number of additional sex chromosomes and the severity of the phenotype is generally assumed. The purpose of this article is to summarize what is known about these conditions and to present 10 additional cases. The karyotypes include, 48,XXXX, 49,XXXXX, 48,XXYY, 48,XXXY, 49,XXXXY, 49,XXXYY, 48,XYYY, 49,XYYYY, and 49,XXYYY.

Mesh:

Year:  1995        PMID: 7567329

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  54 in total

1.  Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy.

Authors:  Anne Marie Ottesen; Lise Aksglaede; Inger Garn; Nicole Tartaglia; Flora Tassone; Claus H Gravholt; Anders Bojesen; Kaspar Sørensen; Niels Jørgensen; Ewa Rajpert-De Meyts; Tommy Gerdes; Anne-Marie Lind; Susanne Kjaergaard; Anders Juul
Journal:  Am J Med Genet A       Date:  2010-05       Impact factor: 2.802

2.  Mortality and cancer incidence in women with extra X chromosomes: a cohort study in Britain.

Authors:  Anthony J Swerdlow; Minouk J Schoemaker; Craig D Higgins; Alan F Wright; Patricia A Jacobs
Journal:  Hum Genet       Date:  2005-11-15       Impact factor: 4.132

Review 3.  Consensus statement on diagnosis and clinical management of Klinefelter syndrome.

Authors:  A F Radicioni; A Ferlin; G Balercia; D Pasquali; L Vignozzi; M Maggi; C Foresta; A Lenzi
Journal:  J Endocrinol Invest       Date:  2010-12       Impact factor: 4.256

4.  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

Review 5.  Effects of sex chromosome aneuploidies on brain development: evidence from neuroimaging studies.

Authors:  Rhoshel K Lenroot; Nancy Raitano Lee; Jay N Giedd
Journal:  Dev Disabil Res Rev       Date:  2009

Review 6.  The cognitive phenotype in Klinefelter syndrome: a review of the literature including genetic and hormonal factors.

Authors:  Richard Boada; Jennifer Janusz; Christa Hutaff-Lee; Nicole Tartaglia
Journal:  Dev Disabil Res Rev       Date:  2009

7.  CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.

Authors:  Abdul Noor; Christian Windpassinger; Megha Patel; Beata Stachowiak; Anna Mikhailov; Matloob Azam; Muhammad Irfan; Zahid Kamal Siddiqui; Farooq Naeem; Andrew D Paterson; Muhammad Lutfullah; John B Vincent; Muhammad Ayub
Journal:  Am J Hum Genet       Date:  2008-04       Impact factor: 11.025

Review 8.  A review of trisomy X (47,XXX).

Authors:  Nicole R Tartaglia; Susan Howell; Ashley Sutherland; Rebecca Wilson; Lennie Wilson
Journal:  Orphanet J Rare Dis       Date:  2010-05-11       Impact factor: 4.123

9.  Diagnosis and mortality in 47,XYY persons: a registry study.

Authors:  Kirstine Stochholm; Svend Juul; Claus H Gravholt
Journal:  Orphanet J Rare Dis       Date:  2010-05-29       Impact factor: 4.123

10.  Detailed analysis of X chromosome inactivation in a 49,XXXXX pentasomy.

Authors:  Lucia M Moraes; Leila Ca Cardoso; Vera Ls Moura; Miguel Am Moreira; Albert N Menezes; Juan C Llerena; Héctor N Seuánez
Journal:  Mol Cytogenet       Date:  2009-10-07       Impact factor: 2.009

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