Literature DB >> 23543039

A Consanguinity Related Autosomal Translocation which Leads to Premature Ovarian Failure.

Mot Yee Yik1, Murizah Mohd Zain, Zubaidah Zakaria, Narazah Mohd Yusoff.   

Abstract

The premature ovarian failures with underlying chromosomal abnormalities are normally X-linked, although their associations with the autosomal and the Robertsonian translocations are also possible. Here, we are reporting a case of premature ovarian failure which was associated with a translocation between the long arm of chromosome 7 at q11.23 and the short arm of chromosome 5 at p15.3. The proband was a 26-year-old Malay woman who presented with premature ovarian failure, who was referred for cytogenetic testing due to the suspicion of a chromosomal anomaly. Her physical examination revealed that she had no abdominal or pelvic masses and that she had normal secondary sexual characteristics. Her medical history as well, revealed no points for concern. However, a consanguineous relationship existed, as the patient's paternal grandmother and maternal grandfather were biological cousins. Our present case indicated that region p15.3 of chromosome 5 and region q11.23 of chromosome 7 possibly carried essential genes for the ovarian function and that they postulated a link between the consanguinity and the chromosomal abnormalities.

Entities:  

Keywords:  Chromosomal abnormality; Consanguinity; Cytogenetic test; Premature ovarian failure; Translocation

Year:  2013        PMID: 23543039      PMCID: PMC3592311          DOI: 10.7860/JCDR/2013/4354.2767

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  10 in total

1.  Autosomal translocation associated with premature ovarian failure.

Authors:  K A Burton; C C Van Ee; K Purcell; I Winship; A N Shelling
Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

2.  Premature ovarian failure associated with a Robertsonian translocation.

Authors:  Y Kawano; H Narahara; N Matsui; I Miyakawa
Journal:  Acta Obstet Gynecol Scand       Date:  1998-04       Impact factor: 3.636

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Journal:  J Med Genet       Date:  1990-06       Impact factor: 6.318

4.  Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions.

Authors:  A T Tharapel; K P Anderson; J L Simpson; P R Martens; R S Wilroy; J C Llerena; C E Schwartz
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

Review 5.  Chromosomal abnormalities in women with premature ovarian failure.

Authors:  Paolo Giovanni Artini; Maria Ruggiero; Francesca Papini; Valeria Valentino; Alessia Uccelli; Vito Cela; Andrea Riccardo Genazzani
Journal:  Gynecol Endocrinol       Date:  2010-10       Impact factor: 2.260

Review 6.  Premature ovarian failure.

Authors:  Deepti Goswami; Gerard S Conway
Journal:  Hum Reprod Update       Date:  2005-05-26       Impact factor: 15.610

Review 7.  Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature.

Authors:  C M Powell; R T Taggart; T C Drumheller; D Wangsa; C Qian; L M Nelson; B J White
Journal:  Am J Med Genet       Date:  1994-08-01

8.  A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus.

Authors:  R A Oldenburg; M F van Dooren; B de Graaf; E Simons; L Govaerts; S Swagemakers; J M H Verkerk; B A Oostra; A M Bertoli-Avella
Journal:  Hum Reprod       Date:  2008-08-09       Impact factor: 6.918

9.  Incidence of premature ovarian failure.

Authors:  C B Coulam; S C Adamson; J F Annegers
Journal:  Obstet Gynecol       Date:  1986-04       Impact factor: 7.661

10.  Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.

Authors:  Sandrine Caburet; Petra Zavadakova; Ziva Ben-Neriah; Kamal Bouhali; Aurélie Dipietromaria; Céline Charon; Céline Besse; Paul Laissue; Vered Chalifa-Caspi; Sophie Christin-Maitre; Daniel Vaiman; Giovanni Levi; Reiner A Veitia; Marc Fellous
Journal:  PLoS One       Date:  2012-03-13       Impact factor: 3.240

  10 in total

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