Literature DB >> 8448906

A case of full triploidy (69,XXX) of paternal origin with unusually long survival time.

S C Niemann-Seyde1, H Rehder, B Zoll.   

Abstract

Triploidy is a rare disorder in live-born children and these infants generally die within the first hours after birth. We report here on a girl with full triploidy and multiple malformations, who survived for 10 1/2 weeks. The extra set of haploid chromosomes was of paternal origin, as shown by chromosomal banding techniques.

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Year:  1993        PMID： 8448906     DOI： 10.1111/j.1399-0004.1993.tb04432.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  4 in total

1.  Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child.

Authors:  J Dean; G Cohen; J Kemp; L Robson; V Tembe; J Hasselaar; B Webster; A Lammi; A Smith
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

2.  Full triploidy in a liveborn preterm infant.

Authors:  K Smets; F Speleman; P Vanhaesebrouck; N Van Roy; J Dehoorne
Journal:  Eur J Pediatr       Date:  1995-08       Impact factor: 3.183

3.  Digynic triploidy: utility and challenges of noninvasive prenatal testing.

Authors:  Julie Fleischer; Archana Shenoy; Katherine Goetzinger; Catherine E Cottrell; Dustin Baldridge; Frances V White; Marwan Shinawi
Journal:  Clin Case Rep       Date:  2015-04-09

4.  Higher limb asymmetry in deceased human fetuses and infants with aneuploidy.

Authors:  Jessica Bots; Clara M A ten Broek; Jeroen A M Belien; Marianna Bugiani; Frietson Galis; Stefan Van Dongen
Journal:  Sci Rep       Date:  2014-01-15       Impact factor: 4.379
  4 in total

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