Literature DB >> 22905310

Discordance between karyotype from amniotic fluid and postnatal lymphocyte cultures.

Domenico Bizzoco1, Ivan Gabrielli, Caterina Tamburrino, Lorena Sonia Carpineto, Alvaro Mesoraca.   

Abstract

Discordance between karyotype seen from amniocentesis and from neonatal blood is a very unusual condition with different possible causes.We present a case of discordance between prenatal cytogenetic diagnosis from amniotic fluid and post-natal cytogenetic diagnosis from lymphocyte cultures.

Keywords:  amniocentesis; array-CGH; karyotype; lymphocyte cultures

Year:  2012        PMID： 22905310      PMCID： PMC3421951     

Source DB:  PubMed          Journal:  J Prenat Med        ISSN： 1971-3282


  5 in total

1.  Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.

Authors:  Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Schu-Rern Chern; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Wayseen Wang
Journal:  Taiwan J Obstet Gynecol       Date:  2011-12       Impact factor: 1.705

2.  Reproductive history of a healthy woman with mosaic duplication of chromosome 4p.

Authors:  Laura Bernardini; Lorenzo Sinibaldi; Caterina Ceccarini; Antonio Novelli; Bruno Dallapiccola
Journal:  Prenat Diagn       Date:  2005-04       Impact factor: 3.050

3.  Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.

Authors:  Sau W Cheung; Chad A Shaw; Daryl A Scott; Ankita Patel; Trilochan Sahoo; Carlos A Bacino; Amber Pursley; Jiangzhen Li; Robert Erickson; Andrea L Gropman; David T Miller; Margretta R Seashore; Anne M Summers; Pawel Stankiewicz; A Craig Chinault; James R Lupski; Arthur L Beaudet; V Reid Sutton
Journal:  Am J Med Genet A       Date:  2007-08-01       Impact factor: 2.802

4.  Discordance between prenatal cytogenetic diagnosis and outcome of pregnancy.

Authors:  A Loft; A Tabor
Journal:  Prenat Diagn       Date:  1984 Jan-Feb       Impact factor: 3.050

5.  An unusual mosaic karyotype detected through prenatal diagnosis with duplication of 1q and 19p and associated teratoma development.

Authors:  S Schwartz; L J Raffel; C C Sun; E Waters
Journal:  Teratology       Date:  1992-10
  5 in total

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