Literature DB >> 29540854

22q11.2 rearrangements found in women with low ovarian reserve and premature ovarian insufficiency.

Sylvie Jaillard1,2,3, Elena J Tucker4,5, Linda Akloul6, Marion Beaumont7, Mathilde Domin8, Laurent Pasquier6, Guilhem Jouve9, Sylvie Odent6, Marc-Antoine Belaud-Rotureau7,10, Célia Ravel10,9.   

Abstract

Ovarian reserve represents the number of available follicles/oocytes within ovaries and it can be assessed by follicle stimulating hormone levels, anti-Müllerian hormone levels, and/or antral follicle count determined by ultrasounds. A low ovarian reserve is defined by an abnormal ovarian reserve test. This condition can be considered premature if it occurs before the age of 40, leading to premature ovarian insufficiency. Despite the growing knowledge concerning the genetic basis of ovarian deficiency, the majority of cases remain without a genetic diagnosis. Although 22q11.2 deletions and duplications have been associated with genitourinary malformations, ovarian deficiency is not a commonly reported feature. We report here four patients bearing a 22q11.2 rearrangement, identified during the clinical assessment of their low ovarian reserve or premature ovarian insufficiency, and discuss the molecular basis of the ovarian defects.

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Year:  2018        PMID: 29540854     DOI: 10.1038/s10038-018-0433-z

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  29 in total

1.  Hypoandrogenism in association with diminished functional ovarian reserve.

Authors:  Norbert Gleicher; Ann Kim; Andrea Weghofer; Vitaly A Kushnir; Aya Shohat-Tal; Emanuela Lazzaroni; Ho-Joon Lee; David H Barad
Journal:  Hum Reprod       Date:  2013-02-20       Impact factor: 6.918

2.  The significance of polymorphism and expression of oestrogen metabolism-related genes in Chinese women with premature ovarian insufficiency.

Authors:  Chunrong Qin; Yong Chen; Qing Lin; Jilong Yao; Weiqing Wu; Jiansheng Xie
Journal:  Reprod Biomed Online       Date:  2017-07-18       Impact factor: 3.828

3.  Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes.

Authors:  S Demczuk; G Thomas; A Aurias
Journal:  Hum Mol Genet       Date:  1996-05       Impact factor: 6.150

4.  Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.

Authors:  Karine Morcel; Tanguy Watrin; Laurent Pasquier; Lucie Rochard; Cédric Le Caignec; Christèle Dubourg; Philippe Loget; Bernard-Jean Paniel; Sylvie Odent; Véronique David; Isabelle Pellerin; Claude Bendavid; Daniel Guerrier
Journal:  Orphanet J Rare Dis       Date:  2011-03-15       Impact factor: 4.123

5.  A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.

Authors:  Sara O Vaz; Renato Pires; Luís M Pires; Isabel M Carreira; Rui Anjos; Paula Maciel; Luisa Mota-Vieira
Journal:  BMC Pediatr       Date:  2015-08-22       Impact factor: 2.125

6.  Deletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role?

Authors:  Veronica Bertini; Alessia Azzarà; Annalisa Legitimo; Roberta Milone; Roberta Battini; Rita Consolini; Angelo Valetto
Journal:  Front Genet       Date:  2017-05-01       Impact factor: 4.599

7.  Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.

Authors:  M De Gregori; R Ciccone; P Magini; T Pramparo; S Gimelli; J Messa; F Novara; A Vetro; E Rossi; P Maraschio; M C Bonaglia; C Anichini; G B Ferrero; M Silengo; E Fazzi; A Zatterale; R Fischetto; C Previderé; S Belli; A Turci; G Calabrese; F Bernardi; E Meneghelli; M Riegel; M Rocchi; S Guerneri; F Lalatta; L Zelante; C Romano; M Fichera; T Mattina; G Arrigo; M Zollino; S Giglio; F Lonardo; A Bonfante; A Ferlini; F Cifuentes; H Van Esch; L Backx; A Schinzel; J R Vermeesch; O Zuffardi
Journal:  J Med Genet       Date:  2007-08-31       Impact factor: 6.318

8.  Investigating the role of X chromosome breakpoints in premature ovarian failure.

Authors:  Simona Baronchelli; Nicoletta Villa; Serena Redaelli; Sara Lissoni; Fabiana Saccheri; Elena Panzeri; Donatella Conconi; Angela Bentivegna; Francesca Crosti; Elena Sala; Francesca Bertola; Anna Marozzi; Antonio Pedicini; Marialuisa Ventruto; Maria Adalgisa Police; Leda Dalprà
Journal:  Mol Cytogenet       Date:  2012-07-16       Impact factor: 2.009

9.  Genotype-phenotype correlation in 22q11.2 deletion syndrome.

Authors:  Elena Michaelovsky; Amos Frisch; Miri Carmel; Miriam Patya; Omer Zarchi; Tamar Green; Lina Basel-Vanagaite; Abraham Weizman; Doron Gothelf
Journal:  BMC Med Genet       Date:  2012-12-17       Impact factor: 2.103

10.  Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.

Authors:  A Norling; A L Hirschberg; K A Rodriguez-Wallberg; E Iwarsson; A Wedell; M Barbaro
Journal:  Hum Reprod       Date:  2014-06-17       Impact factor: 6.918

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  2 in total

1.  Association between chromosome 22q11.2 translocation and male oligozoospermia.

Authors:  Peng Zhan; Tingting Hao; Xiao Yang; Yi Zhang
Journal:  Medicine (Baltimore)       Date:  2022-09-30       Impact factor: 1.817

Review 2.  Genetic determination of the ovarian reserve: a literature review.

Authors:  Aleksandra V Moiseeva; Varvara A Kudryavtseva; Vladimir N Nikolenko; Marine M Gevorgyan; Ara L Unanyan; Anastassia A Bakhmet; Mikhail Y Sinelnikov
Journal:  J Ovarian Res       Date:  2021-08-06       Impact factor: 4.234

  2 in total

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