Literature DB >> 15216553

Nonmosaic smallest duplication of 12q24.31-qter: the first reported case.

Julie Won Ireland1, Syed M Jalal, Pamela S McGrann, Noralane M Lindor.   

Abstract

Duplication of the terminal region of the long arm of chromosome 12 is not common. In 13 previous cases, duplication of this region was generally associated with deletions of the derivative chromosomes, larger sized duplications or mosaicism. We have studied a young man with a nonmosaic duplication of 12q24.31-qter translocated to chromosome 5pter. This is the first reported case of pure subtle duplication involving less than two terminal subbands of 12q24.31 to qter. The origin of this genetic material was confirmed by whole chromosome paints and subtelomere specific FISH probes. As both the subtelomere signals for 5p and 12q were present in the der(5) chromosome, it is unlikely that there was any loss of unique DNA sequences from the terminal region of chromosome 5p. This case is compared with 13 other reported cases with a duplication of the 12q terminal segment. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15216553     DOI: 10.1002/ajmg.a.30098

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Partial Monosomy 4p and Trisomy 12q due to a t(4;12)(p16.3;q24.31) Familial Translocation in Two Cousins.

Authors:  Tatiana Mozer Joaquim; Carlos H Paiva Grangeiro; Flávia Gaona de Oliveira Gennaro; Alexandra Galvão Gomes; Jeremy A Squire; Lucia R Martelli
Journal:  Mol Syndromol       Date:  2019-07-27

2.  7q Deletion/12q Duplication Is the Possible Cause of an Alobar Holoprosencephaly Case.

Authors:  Vassilis Paspaliaris; Nikolaos Vrachnis; Zoe Iliodromiti; Nikolaos Antonakopoulos; Giorgos Papaioannou; Nikolaos Vlachadis; Foteini Anastasiadou; Sotirios Sotiriou; Antonios Garas; Lorreta Thomaidis; Emmanouil Manolakos
Journal:  Mol Syndromol       Date:  2017-11-24
  2 in total

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