Literature DB >> 3966508

Triploidy and chromosomes.

I A Uchida, V C Freeman.   

Abstract

In a total sample of 105 triploid spontaneous abortions and live-born and stillborn infants, the parental origin could be determined in 77%. Dispermy was the most common cause of this abnormality. Among the digynic triploids 69% resulted from retention of the second polar body. Parental ages did not differ from those of the general population except for 10 aneuploid triploids with significantly elevated parental ages. In five sibships, simple aneuploidy in another pregnancy was observed, four of them being potentially viable. Two sisters had triploid conceptions. There were four twin pregnancies, a frequency of one in 26. Only two triploids had an XYY sex chromosome complement, one of which was mosaic with loss of an autosome and the other was a chimera. A frequency of almost 50% of mothers exposed to preconception abdominal radiation is suggestive of an association between radiation and triploidy and requires further investigation.

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Year:  1985        PMID: 3966508     DOI: 10.1016/0002-9378(85)90426-0

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


  14 in total

1.  Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole.

Authors:  M V Zaragoza; U Surti; R W Redline; E Millie; A Chakravarti; T J Hassold
Journal:  Am J Hum Genet       Date:  2000-05-05       Impact factor: 11.025

2.  The genetic risks of in vitro fertilization techniques: the use of an animal model.

Authors:  J Santaló; J Badenas; J M Calafell; V Català; S Munné; J Egozcue; A M Estop
Journal:  J Assist Reprod Genet       Date:  1992-10       Impact factor: 3.412

3.  Phenotypic expression of the first liveborn 68,XX triploid newborn.

Authors:  P Merlob; N Naor; M Shohat
Journal:  J Med Genet       Date:  1991-12       Impact factor: 6.318

4.  Prophase I mouse oocytes are deficient in the ability to respond to fertilization by decreasing membrane receptivity to sperm and establishing a membrane block to polyspermy.

Authors:  Cassie A Kryzak; Maia M Moraine; Diane D Kyle; Hyo J Lee; Caelin Cubeñas-Potts; Douglas N Robinson; Janice P Evans
Journal:  Biol Reprod       Date:  2013-08-29       Impact factor: 4.285

5.  Cytogenetic analysis of in vitro fertilization (IVF) failures.

Authors:  M H Pieters; J P Geraedts; J C Dumoulin; J L Evers; M Bras; F H Kornips; P P Menheere
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

6.  Hydatidiform mole: genetic origin in polyploid conceptuses.

Authors:  L O Vejerslev; J Dissing; H E Hansen; H Poulsen
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

Review 7.  Developmental control of human preimplantation embryos: a comparative approach.

Authors:  J Tesarík
Journal:  J In Vitro Fert Embryo Transf       Date:  1988-12

8.  Parental origin of triploidy in human fetuses: evidence for genomic imprinting.

Authors:  D E McFadden; L C Kwong; I Y Yam; S Langlois
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

9.  Triploidy mosaicism (45,X/68,XX) in an infant presenting with failure to thrive.

Authors:  Jennifer E Posey; Nikki Mohrbacher; Janice L Smith; Ankita Patel; Lorraine Potocki; Amy M Breman
Journal:  Am J Med Genet A       Date:  2015-11-14       Impact factor: 2.802

10.  On the origin of trisomy 21 Down syndrome.

Authors:  Maj A Hultén; Suketu D Patel; Maira Tankimanova; Magnus Westgren; Nikos Papadogiannakis; Anna Maria Jonsson; Erik Iwarsson
Journal:  Mol Cytogenet       Date:  2008-09-18       Impact factor: 2.009

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