Literature DB >> 3362778

An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissue.

J P Crane1, S W Cheung.   

Abstract

While the fetus and placenta have a common ancestry, chorionic villus tissue does not always reflect fetal genotype. Data are presented from 15 CVS subjects in whom cytogenetic inconsistencies were observed when comparing (1) cultured chorionic villi, (2) direct chromosome preparations of intact villi, and (3) cultured fetal tissue. Embryogenic models are presented to explain these discrepancies. Mosaicism confined to direct chromosome preparations was the most commonly observed inconsistency. This can be explained by postzygotic non-disjunction limited to cytotrophoblast. In all but one instance, the abnormal cell line was limited to the placenta, with the normal cell line reflecting fetal genotype. Analysis of direct chromosome preparations from multiple individually processed villus fragments may be helpful in recognizing mosaicism confined to the placenta. While both direct chromosome preparations and villus cultures can be misleading, the latter are more likely to reflect fetal genetic status since they are derived from the extraembryonic mesoderm.

Mesh:

Year:  1988        PMID: 3362778     DOI: 10.1002/pd.1970080206

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  9 in total

1.  A case of apparent trisomy 21 without the Down's syndrome phenotype.

Authors:  D Avramopoulos; I Kennerknecht; G Barbi; D Eckert; J M Delabar; C Maunoury; A Hallberg; M B Petersen
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

Review 2.  Biological characteristics of stem cells from foetal, cord blood and extraembryonic tissues.

Authors:  Hassan Abdulrazzak; Dafni Moschidou; Gemma Jones; Pascale V Guillot
Journal:  J R Soc Interface       Date:  2010-08-25       Impact factor: 4.118

3.  Three different, non-mosaic sex chromosome abnormalities (direct cytotrophoblasts, mesenchymal core cultures, and abortus skin fibroblasts): implications for elucidating chorionic villi mosaicism.

Authors:  L P Shulman; A T Tharapel; J L Simpson; C M Meyers; B Tucker; B Weisskopf; S Elias
Journal:  J Med Genet       Date:  1989-12       Impact factor: 6.318

Review 4.  Review and hypotheses: somatic mosaicism: observations related to clinical genetics.

Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

5.  A chimaeric animal model for confined placental mosaicism.

Authors:  R M James; J D West
Journal:  Hum Genet       Date:  1994-05       Impact factor: 4.132

6.  X chromosome inactivation and the diagnosis of X linked disease in females.

Authors:  R M Brown; G K Brown
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

7.  Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG).

Authors:  Athena M Cherry; Yassmine M Akkari; Kimberly M Barr; Hutton M Kearney; Nancy C Rose; Sarah T South; James H Tepperberg; Jeanne M Meck
Journal:  Genet Med       Date:  2017-07-20       Impact factor: 8.822

Review 8.  Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis.

Authors:  Francesca Romana Grati
Journal:  J Clin Med       Date:  2014-07-24       Impact factor: 4.241

Review 9.  False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review.

Authors:  Diane Van Opstal; Malgorzata I Srebniak; Joke Polak; Femke de Vries; Lutgarde C P Govaerts; Marieke Joosten; Attie T J I Go; Maarten F C M Knapen; Cardi van den Berg; Karin E M Diderich; Robert-Jan H Galjaard
Journal:  PLoS One       Date:  2016-01-15       Impact factor: 3.240

  9 in total

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