Literature DB >> 7449187

Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughter.

V G Kirkels, T W Hustinx, J M Scheres.   

Abstract

This paper describes the unexpected transmission of a translocation (22;22)(p13;q11) from a mother to her phenotypically normal daughter (the proband). Both women had had multiple abortions. No signs of mosaicism with respect to chromosome No. 22 were found in the proband or in her mother. Until now, it has been generally assumed that carriers of a 22/22 translocation will have only abnormal conceptuses. The transmission of this translocation from a balanced carrier to a phenotypically normal daughter was therefore highly unexpected and is not easy to explain. Early postzygotic loss of a chromosome no. 22 from a trisomic zygote, or fertilization of an oocyte carrying the translocation by a sperm nullisomic for chromosome no. 22 could have led to the balanced chromosome pattern of the proband.

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Year:  1980        PMID: 7449187     DOI: 10.1111/j.1399-0004.1980.tb01794.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  26 in total

1.  Uniparental disomy and gene localization.

Authors:  A A Schinzel
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025

2.  Homologous Robertsonian translocation (21q21q) and abortions.

Authors:  T Sudha; P M Gopinath
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

3.  Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?

Authors:  R Voss; E Ben-Simon; A Avital; S Godfrey; J Zlotogora; J Dagan; Y Tikochinski; J Hillel
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

4.  Chromosomal basis of recurrent fetal losses.

Authors:  A T Tharapel; R S Wilroy
Journal:  Indian J Pediatr       Date:  1986 Jul-Aug       Impact factor: 1.967

5.  Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism.

Authors:  N Créau-Goldberg; A Gegonne; J Delabar; C Cochet; M O Cabanis; D Stehelin; C Turleau; J de Grouchy
Journal:  Hum Genet       Date:  1987-08       Impact factor: 4.132

6.  Cytogenetic contribution to uniparental disomy (UPD).

Authors:  Thomas Liehr
Journal:  Mol Cytogenet       Date:  2010-03-29       Impact factor: 2.009

7.  Maternal uniparental disomy 22 has no impact on the phenotype.

Authors:  A A Schinzel; S Basaran; F Bernasconi; B Karaman; M Yüksel-Apak; W P Robinson
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025

8.  Normal phenotype with paternal uniparental isodisomy for chromosome 21.

Authors:  J L Blouin; D Avramopoulos; C Pangalos; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

9.  Trisomy 22 in a newborn with multiple malformations.

Authors:  I Voiculescu; E Back; A M Duncan; H Schwaibold; W Schempp
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

10.  Molecular studies of DiGeorge syndrome.

Authors:  W J Fibison; M Budarf; H McDermid; F Greenberg; B S Emanuel
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

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