Literature DB >> 12123494

Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases.

Katja Eggermann1, U A Mau, G Bujdosó, E Koltai, H Engels, R Schubert, T Eggermann, R Raff, G Schwanitz.   

Abstract

Small supernumerary marker chromosomes (SMC) are a heterogeneous group of chromosomes with an estimated frequency of approximately 0.14-0.72 per 1000 newborns and higher frequencies in particular populations such as the mentally retarded or infertile males. With a frequency of about 50%, derivatives of chromosome 15 represent the most common SMC. Here we present the results of a detailed analysis of 32 SMC(15) carriers who were ascertained in pre- or post-natal routine cytogenetic diagnostics. SMC(15) with euchromatic content led to mental and psychomotor retardation. In contrast, SMC(15) without euchromatin were found to have no influence on the carrier's phenotype but were detected with a high incidence among infertile males. The majority of SMC(15) are pseudodicentric homologous rearrangements. Based on our investigations a further characterization of der(15) was possible.

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Year:  2002        PMID: 12123494     DOI: 10.1034/j.1399-0004.2002.620113.x

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


  14 in total

1.  High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage.

Authors:  Nicholas J Wang; Dahai Liu; Alexander S Parokonny; N Carolyn Schanen
Journal:  Am J Hum Genet       Date:  2004-06-11       Impact factor: 11.025

2.  Infertility and marker chromosomes: application of molecular cytogenetic techniques in a case of inv dup(15).

Authors:  Tania M Vulcani-Freitas; Vera L Gil-da-Silva-Lopes; Marileila Varella-Garcia; Andréa T Maciel-Guerra
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

3.  Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.

Authors:  Dorota A Kwasnicka-Crawford; Wendy Roberts; Stephen W Scherer
Journal:  J Autism Dev Disord       Date:  2007-04

4.  Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues.

Authors:  Erin L Baldwin; Lorraine F May; April N Justice; Christa L Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2008-02       Impact factor: 11.025

5.  A case of an infertile male with a small supernumerary marker chromosome negative for M-FISH and containing only heterochromatin.

Authors:  Wei Wang; Yali Hu; Haiyan Zhu; Jie Li; Ruifang Zhu; Ya-Ping Wang
Journal:  J Assist Reprod Genet       Date:  2009-05-14       Impact factor: 3.412

6.  Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformity.

Authors:  Altuğ Koç; S Odül Onur; Mehmet Ali Ergün; E Ferda Perçin
Journal:  Asian J Androl       Date:  2009-08-24       Impact factor: 3.285

7.  Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity.

Authors:  S E Roberts; F Maggouta; N S Thomas; P A Jacobs; J A Crolla
Journal:  Am J Hum Genet       Date:  2003-10-14       Impact factor: 11.025

Review 8.  Chromosome abnormalities without phenotypic consequences.

Authors:  Małgorzata Kowalczyk; Małgorzata Srebniak; Agnieszka Tomaszewska
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

9.  Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy.

Authors:  S M Mann; N J Wang; D H Liu; L Wang; R A Schultz; N Dorrani; M Sigman; N C Schanen
Journal:  Hum Genet       Date:  2004-05-13       Impact factor: 4.132

Review 10.  A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.

Authors:  Jörg Seidel; Anita Heller; Gabriele Senger; Heike Starke; Ilse Chudoba; Christina Kelbova; Holger Tönnies; Heidemarie Neitzel; Claudia Haase; Volkmar Beensen; Felix Zintl; Uwe Claussen; Thomas Liehr
Journal:  Eur J Pediatr       Date:  2003-06-19       Impact factor: 3.183

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