Literature DB >> 8766143

Parental origin of the extra chromosome 18 in Edwards syndrome.

K H Ramesh1, R S Verma.   

Abstract

Trisomy 18 (Edwards syndrome) is the second most common trisomy in human. The parental origin of the additional chromosome leading to meiotic errors is imperative to understand the etiology of trisomy 18. We compiled the data on 171 cases (table I) where meiotic error is provided. The paternal meiotic error occurred in 7% of the cases while in 93% of the cases nondisjunction took place in the mother. There were 28 cases (16%) where nondisjunction took place in meiosis I(MI), 53 cases (31%) in meiosis II (MII) and in 90 cases (53%) either the error was postzygotic mitosis or the dysfunctional stages could not be determined. The age distribution could be found in 119 cases (table II) and a conclusion could not be drawn as there were only 11 cases where paternal nondisjunction was noted.

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Year:  1996        PMID: 8766143

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  3 in total

1.  Sperm ultrastructure and 18, X, Y aneuploidies in a man with a 46 XY, 47 XY + 18 mosaic karyotype: case report.

Authors:  G Collodel; I Cosci; A N Pascarelli; E Moretti
Journal:  J Assist Reprod Genet       Date:  2007-07-17       Impact factor: 3.412

2.  Shedding Light on the Nature of Seminal Round Cells.

Authors:  Gianpiero D Palermo; Queenie V Neri; Tyler Cozzubbo; Stephanie Cheung; Nigel Pereira; Zev Rosenwaks
Journal:  PLoS One       Date:  2016-03-16       Impact factor: 3.240

3.  Congenital hydrocephalus in an Egyptian baby with trisomy 18: a case report.

Authors:  Kotb A Metwalley; Hekma S Farghalley; Alaa A Abd-Elsayed
Journal:  J Med Case Rep       Date:  2009-11-09
  3 in total

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