Literature DB >> 11484205

Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter.

Y S Fan1, V M Siu.   

Abstract

A derivative chromosome 8 was observed in a newborn boy who presented with low birth weight, multiple congenital anomalies, and dysmorphic face. The der(8) was further characterized at age 18 months by a high resolution G-banding analysis, spectral karyotyping, and fluorescence in situ hybridization (FISH) with multiple DNA probes. The karyotype was described as 46,XY,der(8)(qter-->q24.13::p21.3-->p23.3::p23.3-->qter), representing an inverted duplication of region 8p21.3-->p23.3 and a duplication of region 8q24.13-->qter, which attaches to the duplicated short arm segment at 8p21.3. Different from previously reported patients with an inverted duplication (8p), no deletion was detected in the distal region of 8p in this case. This young child had manifested a broad nasal bridge, micrognathia, cleft lip, hydrocephalus, partial agenesis of the corpus callosum, Dandy-Walker malformation, congenital heart defects, dysplastic kidneys, hydronephrosis, marked hypotonia, and significant psychomotor retardation. These features are compared with those commonly seen in cases with an inverted duplication of 8p and cases with a partial trisomy of 8q. Copyright 2001 Wiley-Liss, Inc.

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Mesh:

Year:  2001        PMID: 11484205     DOI: 10.1002/ajmg.1460

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 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.  FGF17, a gene involved in cerebellar development, is downregulated in a patient with Dandy-Walker malformation carrying a de novo 8p deletion.

Authors:  Ginevra Zanni; Sabina Barresi; Lorena Travaglini; Laura Bernardini; Teresa Rizza; Maria Cristina Digilio; Eugenio Mercuri; Stefano Cianfarani; Massimiliano Valeriani; Alessandro Ferraris; Letizia Da Sacco; Antonio Novelli; Enza Maria Valente; Bruno Dallapiccola; Enrico Silvio Bertini
Journal:  Neurogenetics       Date:  2011-04-12       Impact factor: 2.660

3.  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

4.  A 9p13-->p24 duplication coupled with a whole 22q translocation onto 9p24.

Authors:  Horacio Rivera; Ana I Vásquez-Velásquez; Mariá de Lourdes Ramirez-Duenas; Luis Eduardo Becerra-Solano
Journal:  J Appl Genet       Date:  2007       Impact factor: 2.653

5.  Selection in the evolution of gene duplications.

Authors:  Fyodor A Kondrashov; Igor B Rogozin; Yuri I Wolf; Eugene V Koonin
Journal:  Genome Biol       Date:  2002-01-14       Impact factor: 13.583

  5 in total

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