Literature DB >> 16103660

Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.

A Polityko1, H Starke, N Rumyantseva, U Claussen, T Liehr, S Raskin.   

Abstract

In this report, we describe three unrelated patients with similar symptoms such as mental retardation, growth delay and multiple phenotypic abnormalities. GTG-banding analysis revealed karyotypes with add(1p) in two cases and an add(1q) in the third. Fluorescence in situ hybridization (FISH) analysis using high resolution multicolor banding (MCB) characterized the aberrations of the abnormal chromosomes 1 as a (sub)terminal duplication and inverted duplications, respectively. Although three different chromosomal regions i.e. 1p36.1, 1p36.2-->1p31.3 and 1q41-->1q44 were involved, all three patients had similar patterns of dysmorphic findings. These cases demonstrate the power of MCB in the characterization of small interstitial chromosomal aberrations and resulted in the characterization of three previously unreported congenital chromosome 1 rearrangements.

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Year:  2005        PMID: 16103660     DOI: 10.1159/000086388

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  6 in total

1.  Proteinuric glomerulopathy in an adolescent with a distal partial trisomy chromosome 1.

Authors:  Takaya Sasaki; Masahiro Okabe; Takeshi Tosaki; Yu Honda; Masahiro Ishikawa; Nobuo Tsuboi; Takashi Yokoo
Journal:  CEN Case Rep       Date:  2018-05-16

2.  Partial 1q Duplications and Associated Phenotype.

Authors:  Marcos L M Morris; José E Baroneza; Patricia Teixeira; Cristina T N Medina; Mara S Cordoba; Beatriz R Versiani; Liege L Roese; Erika L Freitas; Ana C S Fonseca; Maria C G Dos Santos; Aline Pic-Taylor; Carla Rosenberg; Silviene F Oliveira; Iris Ferrari; Juliana F Mazzeu
Journal:  Mol Syndromol       Date:  2016-02-04

3.  Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up.

Authors:  Vera Ayres Meloni; Sylvia Satomi Takeno; Ana Luiza Pilla; Claudia Berlim de Mello; Maria Isabel Melaragno; Leslie Domenici Kulikowski
Journal:  Mol Cytogenet       Date:  2014-08-22       Impact factor: 2.009

4.  Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.

Authors:  Alicia Cervantes; Constanza García-Delgado; Fernando Fernández-Ramírez; Carolina Galaz-Montoya; Ariadna Berenice Morales-Jiménez; Karem Nieto-Martínez; Laura Gómez-Laguna; Judith Villa-Morales; Mónica Quintana-Palma; Jaime Berúmen; Susana Kofman; Verónica F Morán-Barroso
Journal:  BMC Med Genomics       Date:  2014-09-15       Impact factor: 3.063

5.  Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies: A case report.

Authors:  Beata Aleksiūnienė; Rugilė Matulevičiūtė; Aušra Matulevičienė; Birutė Burnytė; Natalija Krasovskaja; Laima Ambrozaitytė; Violeta Mikštienė; Vaidas Dirsė; Algirdas Utkus; Vaidutis Kučinskas
Journal:  Medicine (Baltimore)       Date:  2017-04       Impact factor: 1.889

6.  Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings.

Authors:  Aixiang Luo; Dehua Cheng; Shimin Yuan; Haiyu Li; Juan Du; Yang Zhang; Chuanchun Yang; Ge Lin; Wenyong Zhang; Yue-Qiu Tan
Journal:  Mol Cytogenet       Date:  2018-04-04       Impact factor: 2.009

  6 in total

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