Literature DB >> 1740326

The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.

P Simi1, M Ceccarelli, A Barachini, G Floridia, O Zuffardi.   

Abstract

Carriers of the standard translocation t(11;22) (q23.3;q11.2) produce only one type of unbalanced offspring, a tertiary trisomy resulting into the karyotype 47,XX or XY, +der(22)t(11;22)(q23.3;q11.2), usually derived from the mother. The exception is one single patient 47,XY,t(11;22)(q23.3;q11.2), +der(22)t(11;22) (q23.3;q11.2)pat. We report a second case with the same karyotype, also of paternal origin. Thus, the rare unbalanced offspring of a carrier father (only 5 cases known) may receive a supernumerary der(22), as a consequence of tertiary trisomy, but also as a consequence of nondisjunction at meiosis II of a balanced spermatocyte.

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Year:  1992        PMID: 1740326     DOI: 10.1007/bf00215688

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  7 in total

1.  Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.

Authors:  D H Lockwood; A Farrier; F Hecht; J Allanson
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

2.  The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families.

Authors:  L Iselius; J Lindsten; A Aurias; M Fraccaro; C Bastard; A M Bottelli; T H Bui; D Caufin; L Dalprà; N Delendi
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  Further studies on chiasma distribution and interference in the human male.

Authors:  D A Laurie; M A Hultén
Journal:  Ann Hum Genet       Date:  1985-07       Impact factor: 1.670

4.  Further studies on bivalent chiasma frequency in human males with normal karyotypes.

Authors:  D A Laurie; M A Hultén
Journal:  Ann Hum Genet       Date:  1985-07       Impact factor: 1.670

5.  The 11q;22q translocation: a European collaborative analysis of 43 cases.

Authors:  M Fraccaro; J Lindsten; C E Ford; L Iselius
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

6.  The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.

Authors:  A Schinzel; W Schmid; M Fraccaro; L Tiepolo; O Zuffardi; J M Opitz; J Lindsten; P Zetterqvist; H Enell; C Baccichetti; R Tenconi; R A Pagon
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Characterization of the supernumerary chromosome in cat eye syndrome.

Authors:  H E McDermid; A M Duncan; K R Brasch; J J Holden; E Magenis; R Sheehy; J Burn; N Kardon; B Noel; A Schinzel
Journal:  Science       Date:  1986-05-02       Impact factor: 47.728

  7 in total
  5 in total

1.  Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families.

Authors:  T H Shaikh; M L Budarf; L Celle; E H Zackai; B S Emanuel
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

2.  Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.

Authors:  S J Armstrong; A S Goldman; R M Speed; M A Hultén
Journal:  Am J Hum Genet       Date:  2000-08-08       Impact factor: 11.025

3.  Involvement of 3:1 disjunction in the common reciprocal translocation t(11;22) (q23.3;q11.2)

Authors:  A C Chandley
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

4.  A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.

Authors:  Vaidehi Jobanputra; Wendy K Chung; April M Hacker; Beverly S Emanuel; Dorothy Warburton
Journal:  Prenat Diagn       Date:  2005-08       Impact factor: 3.050

5.  Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.

Authors:  A J Dawson; A J Mears; A E Chudley; T Bech-Hansen; H McDermid
Journal:  J Med Genet       Date:  1996-11       Impact factor: 6.318

  5 in total

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