Literature DB >> 1997383

Frequency and distribution of aneuploidy in human female gametes.

F Pellestor1.   

Abstract

During the past 6 years, 14 cytogenetic studies on human oocytes recovered during in vitro fertilization procedures have been published; they report contradictory results. The present survey has pooled the more than 1500 oocyte chromosome complements examined to date, in order to determine generalized trends in chromosomal abnormalities of female gametes. The overall frequency of abnormalities in mature oocytes is 24.0% with a large majority of aneuploidies (22.8%) over structural aberrations (1.2%), which could be explained by the difficulty in the detection of structural abnormalities in oocyte chromosome sets. An analysis of the distribution of non-disjunction among all chromosomes was also performed. In the A, C, D, and especially in the G groups, there is a significant difference between the observed non-disjunction and the frequencies expected from an equal partitioning of non-disjunction among all chromosomes. These data are discussed with reference to the differences obtained from cytogenetic studies on human sperm and from investigations on spontaneous abortion.

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Year:  1991        PMID: 1997383     DOI: 10.1007/bf00202410

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


  45 in total

1.  Origin of the extra chromosome in trisomy 21.

Authors:  J F Mattei; M G Mattei; S Ayme; F Giraud
Journal:  Hum Genet       Date:  1979-01-19       Impact factor: 4.132

2.  An improved, efficient method for analyzing human sperm chromosomes using zona-free hamster ova.

Authors:  Y Kamiguchi; K Mikamo
Journal:  Am J Hum Genet       Date:  1986-05       Impact factor: 11.025

3.  Cytogenetic investigations on human oocytes and early human embryonic stages.

Authors:  H W Michelmann; L Mettler
Journal:  Fertil Steril       Date:  1985-02       Impact factor: 7.329

4.  Cytogenetic analysis of living human oocytes: cellular basis and developmental consequences of perturbations in chromosomal organization and complement.

Authors:  J Van Blerkom; G Henry
Journal:  Hum Reprod       Date:  1988-08       Impact factor: 6.918

5.  Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

Authors:  R C Juberg; P N Mowrey
Journal:  Am J Med Genet       Date:  1983-09

6.  Are clinical and biological IVF parameters correlated with chromosomal disorders in early life: a multicentric study.

Authors:  M Plachot; A Veiga; J Montagut; J de Grouchy; G Calderon; S Lepretre; A M Junca; J Santalo; E Carles; J Mandelbaum
Journal:  Hum Reprod       Date:  1988-07       Impact factor: 6.918

7.  Chromosomes of human sperm: variability among normal individuals.

Authors:  B Brandriff; L Gordon; L Ashworth; G Watchmaker; D Moore; A J Wyrobek; A V Carrano
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Nucleolus, nucleolar chromosomes, and nucleolus-associated chromatin from early diplotene to dictyotene in the human oocyte.

Authors:  A M Vagner-Capodano; M Hartung; A Stahl
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

9.  Chromosome anomalies in human oocytes failing to fertilize after insemination in vitro.

Authors:  A Bongso; N S Chye; S Ratnam; H Sathananthan; P C Wong
Journal:  Hum Reprod       Date:  1988-07       Impact factor: 6.918

10.  Origin of extra chromosome in Patau syndrome.

Authors:  S Ishikiriyama; N Niikawa
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

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  16 in total

1.  Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down syndrome: increased incidence in cases of paternal origin.

Authors:  J Blanco; E Gabau; D Gómez; N Baena; M Guitart; J Egozcue; F Vidal
Journal:  Am J Hum Genet       Date:  1998-10       Impact factor: 11.025

Review 2.  The control of mammalian female meiosis: factors that influence chromosome segregation.

Authors:  P A Hunt
Journal:  J Assist Reprod Genet       Date:  1998-05       Impact factor: 3.412

3.  Cytogenetic analysis of human oocytes parthenogenetically activated by puromycin.

Authors:  P De Sutter; D Dozortsev; P Vrijens; R Desmet; M Dhont
Journal:  J Assist Reprod Genet       Date:  1994-09       Impact factor: 3.412

4.  Chromosomal analysis of unfertilized human oocytes prepared by a gradual fixation-air drying method.

Authors:  Y Kamiguchi; B Rosenbusch; K Sterzik; K Mikamo
Journal:  Hum Genet       Date:  1993-01       Impact factor: 4.132

5.  Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction.

Authors:  E L Spriggs; A W Rademaker; R H Martin
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025

6.  A fluorescent in situ hybridization analysis of X chromosome pairing in early human female meiosis.

Authors:  Y E Cheng; S M Gartler
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

7.  A 45,X/46,XX/47,XXX female mosaic detected by cytogenetic analysis of unfertilized IVF oocytes.

Authors:  P De Sutter; M Dhont; E Merchiers; T Coetsier; M R Verschraegen-Spae; M Coppens
Journal:  J Assist Reprod Genet       Date:  1993-08       Impact factor: 3.412

8.  Detection of aneuploidy in human oocytes and corresponding first polar bodies by fluorescent in situ hybridization.

Authors:  A Dyban; M Freidine; E Severova; J Cieslak; V Ivakhnenko; Y Verlinsky
Journal:  J Assist Reprod Genet       Date:  1996-01       Impact factor: 3.412

9.  Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.

Authors:  P Höglund; C Holmberg; A de la Chapelle; J Kere
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

10.  Meiotic recombination in human oocytes.

Authors:  Edith Y Cheng; Patricia A Hunt; Theresa A Naluai-Cecchini; Corrine L Fligner; Victor Y Fujimoto; Tanya L Pasternack; Jackie M Schwartz; Jody E Steinauer; Tracey J Woodruff; Sheila M Cherry; Terah A Hansen; Rhea U Vallente; Karl W Broman; Terry J Hassold
Journal:  PLoS Genet       Date:  2009-09-18       Impact factor: 5.917

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