Literature DB >> 18460934

Fragile X and reproduction.

J Ryan Martin1, Aydin Arici.   

Abstract

PURPOSE OF REVIEW: To review the recent literature on fragile X and the genotypic and phenotypic implications on human reproduction. RECENT
FINDINGS: Fragile X syndrome is the most common inherited cause of mental retardation and the most common genetic cause of autism. The fully expanded form of the mutation leads to mental retardation and autism, whereas the premutation can lead to a neurological disorder called fragile X-associated tremor/ataxia, macroorchidism after puberty and premature ovarian failure. Fragile X is also a major cause of premature ovarian failure and irregular menses, and it can subsequently affect fertility. Couples who carry the premutation or full mutation should be offered genetic and preconceptual counseling prior to attempting to conceive. This allows the patient full disclosure about the risks of transmitting the mutation and possible preventive measures, which allows them to formulate educated decisions about their reproductive future.
SUMMARY: Clinicians should identify and recognize clinical situations that warrant fragile X testing to properly counsel and inform patients about their reproductive possibilities and ways to increase their chances of a successful reproductive outcome.

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Year:  2008        PMID: 18460934     DOI: 10.1097/GCO.0b013e3282fe7254

Source DB:  PubMed          Journal:  Curr Opin Obstet Gynecol        ISSN: 1040-872X            Impact factor:   1.927


  11 in total

1.  Preimplantation genetic diagnosis versus prenatal diagnosis-decision-making among pregnant FMR1 premutation carriers.

Authors:  Lilach Marom Haham; Inbal Avrahami; Noam Domniz; Liat Ries-Levavi; Michal Berkenstadt; Raoul Orvieto; Yoram Cohen; Shai E Elizur
Journal:  J Assist Reprod Genet       Date:  2018-08-22       Impact factor: 3.412

2.  Are expanded alleles of the FMR1 gene related to unexplained recurrent miscarriages?

Authors:  M Fragkos; H Bili; D Ntelios; G Tzimagiorgis; B C Tarlatzis
Journal:  Hippokratia       Date:  2018 Jul-Sep       Impact factor: 0.471

Review 3.  Fragile X syndrome.

Authors:  Wilmar Saldarriaga; Flora Tassone; Laura Yuriko González-Teshima; Jose Vicente Forero-Forero; Sebastián Ayala-Zapata; Randi Hagerman
Journal:  Colomb Med (Cali)       Date:  2014-12-30

4.  X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation.

Authors:  Susana I Ferreira; Eunice Matoso; Marta Pinto; Joana Almeida; Thomas Liehr; Joana B Melo; Isabel M Carreira
Journal:  Mol Cytogenet       Date:  2010-07-20       Impact factor: 2.009

Review 5.  Childhood developmental disorders: an academic and clinical convergence point for psychiatry, neurology, psychology and pediatrics.

Authors:  Allan L Reiss
Journal:  J Child Psychol Psychiatry       Date:  2009-01       Impact factor: 8.982

6.  An explanation of the mechanisms underlying fragile X-associated premature ovarian insufficiency.

Authors:  Bruce I Rose; Samuel E Brown
Journal:  J Assist Reprod Genet       Date:  2020-05-06       Impact factor: 3.412

7.  Fragile X Premutation Carrier Epidemiology and Symptomatology in Israel-Results from a Tertiary Child Developmental Center.

Authors:  Lidia V Gabis; Noah Gruber; Michal Berkenstadt; Shahar Shefer; Odelia Leon Attia; Dana Mula; Yoram Cohen; Shai E Elizur
Journal:  Cerebellum       Date:  2016-10       Impact factor: 3.847

Review 8.  Fragile X-Associated Diminished Ovarian Reserve and Primary Ovarian Insufficiency from Molecular Mechanisms to Clinical Manifestations.

Authors:  Limor Man; Jovana Lekovich; Zev Rosenwaks; Jeannine Gerhardt
Journal:  Front Mol Neurosci       Date:  2017-09-12       Impact factor: 5.639

9.  Expanded alleles of the FMR1 gene are related to unexplained recurrent miscarriages.

Authors:  Xin-Hua Wang; Xiao-Hua Song; Yan-Lin Wang; Xing-Hua Diao; Tong Li; Qing-Chun Li; Xiang-Hui Zhang; Xiao-Hui Deng
Journal:  Biosci Rep       Date:  2017-11-23       Impact factor: 3.840

10.  Premature recruitment of oocyte pool and increased mTOR activity in Fmr1 knockout mice and reversal of phenotype with rapamycin.

Authors:  E Mok-Lin; M Ascano; A Serganov; Z Rosenwaks; T Tuschl; Z Williams
Journal:  Sci Rep       Date:  2018-01-12       Impact factor: 4.379

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