Literature DB >> 19041960

Unusual 8p inverted duplication deletion with telomere capture from 8q.

Karen Buysse1, Francesca Antonacci, Bert Callewaert, Bart Loeys, Ulrike Fränkel, Victoria Siu, Geert Mortier, Frank Speleman, Björn Menten.   

Abstract

Inverted 8p duplication deletions are recurrent chromosomal rearrangements that are mediated through non-allelic homologous recombination (NAHR) between olfactory receptor (OR) gene clusters at 8p23.1. These rearrangements result in a proximal inverted duplication of various extent, a single copy region between the OR gene clusters and a terminal 8p deletion. The terminal deletions are stabilized by direct addition of telomeric repeats, so called telomere healing. Here, we report a patient with an unusual inverted duplication deletion of 8p. Stabilization of the broken chromosome end was achieved by telomere capture instead of telomere healing, resulting in an additional duplication of 8q24.13-->qter on the short arm of chromosome 8. Moreover, the inverted duplication was only 3.4 Mb in size (restricted to band 8p22) and thus cytogenetically undetectable. To the best of our knowledge this is the smallest inverted duplication reported hitherto. We describe the molecular characterization by FISH and array CGH of this unusual inv dup del (8p) and a previously reported patient with a similar 8q duplication and review the literature on cases associated with telomere capture.

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Year:  2008        PMID: 19041960     DOI: 10.1016/j.ejmg.2008.10.007

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  8 in total

1.  De novo unbalanced translocations have a complex history/aetiology.

Authors:  Maria Clara Bonaglia; Nehir Edibe Kurtas; Edoardo Errichiello; Sara Bertuzzo; Silvana Beri; Mana M Mehrjouy; Aldesia Provenzano; Debora Vergani; Vanna Pecile; Francesca Novara; Paolo Reho; Marilena Carmela Di Giacomo; Giancarlo Discepoli; Roberto Giorda; Micheala A Aldred; Cíntia Barros Santos-Rebouças; Andressa Pereira Goncalves; Diane N Abuelo; Sabrina Giglio; Ivana Ricca; Fabrizia Franchi; Philippos Patsalis; Carolina Sismani; María Angeles Morí; Julián Nevado; Niels Tommerup; Orsetta Zuffardi
Journal:  Hum Genet       Date:  2018-10-01       Impact factor: 4.132

2.  Genotype-phenotype association studies of chromosome 8p inverted duplication deletion syndrome.

Authors:  Gene S Fisch; Ryan Davis; Janey Youngblom; Jeff Gregg
Journal:  Behav Genet       Date:  2011-01-23       Impact factor: 2.805

3.  Genomic profile of copy number variants on the short arm of human chromosome 8.

Authors:  Shihui Yu; Stephanie Fiedler; Andrew Stegner; William D Graf
Journal:  Eur J Hum Genet       Date:  2010-05-12       Impact factor: 4.246

4.  Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report.

Authors:  Dilek Aktas; Anja Weise; Eda Utine; Dursun Alehan; Kristin Mrasek; Ferdinand von Eggeling; Heike Thieme; Ergul Tuncbilek; Thomas Liehr
Journal:  Mol Cytogenet       Date:  2009-06-30       Impact factor: 2.009

5.  Phenotypic and molecular insights into CASK-related disorders in males.

Authors:  Ute Moog; Tatjana Bierhals; Kristina Brand; Jan Bautsch; Saskia Biskup; Thomas Brune; Jonas Denecke; Christine E de Die-Smulders; Christina Evers; Maja Hempel; Marco Henneke; Helger Yntema; Björn Menten; Joachim Pietz; Rolph Pfundt; Jörg Schmidtke; Doris Steinemann; Constance T Stumpel; Lionel Van Maldergem; Kerstin Kutsche
Journal:  Orphanet J Rare Dis       Date:  2015-04-12       Impact factor: 4.123

6.  De Novo San Luis Valley Syndrome-like der(8) Chromosome With a Concomitant dup(8p22) in a Mexican Girl.

Authors:  Alma Laura Sánchez-Casillas; Horacio Rivera; Anna Gabriela Castro-Martínez; José Elías García-Ortiz; Carlos Córdova-Fletes; Paul Mendoza-Pérez
Journal:  Ann Lab Med       Date:  2017-01       Impact factor: 3.464

7.  Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features.

Authors:  Jacquelyn D Riley; Catherine M Stefaniuk; Francine Erenberg; Angelika L Erwin; Lauren Palange; Caroline Astbury
Journal:  Case Rep Genet       Date:  2019-07-25

8.  Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region.

Authors:  Serena Redaelli; Donatella Conconi; Elena Sala; Nicoletta Villa; Francesca Crosti; Gaia Roversi; Ilaria Catusi; Chiara Valtorta; Maria Paola Recalcati; Leda Dalprà; Marialuisa Lavitrano; Angela Bentivegna
Journal:  Int J Mol Sci       Date:  2022-03-20       Impact factor: 5.923

  8 in total

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