Literature DB >> 21466863

A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia.

Jill K Northup1, Reuben Matalon, Lillian H Lockhart, Judy C Hawkins, Gopalrao V N Velagaleti.   

Abstract

Complex chromosome rearrangements (CCRs) are structural abnormalities involving >2 chromosomes or >3 breakpoints. It has been suggested that the probability of imbalance increases as the number of breakpoints increase. Here we report a 7-month-old, Hispanic girl presenting with cleidocranial dysplasia (CCD) who was found to have a complex chromosome rearrangement of chromosome 6. Fluorescence in situ hybridization studies with bacterial artificial chromosome (BAC) clones showed that the rearrangement involved insertion of 6q into 6p disrupting the "Runt related transcription factor 2 (RUNX2)" gene at chromosome 6p21.1. In addition, a pericentric inversion of chromosome 6 was identified. Despite the complex nature of the rearrangement, no cryptic deletions or duplications could be detected by array comparative genomic hybridization.
Copyright © 2011 Elsevier Masson SAS. All rights reserved.

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Year:  2011        PMID: 21466863     DOI: 10.1016/j.ejmg.2011.03.011

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


  4 in total

1.  The promise of human induced pluripotent stem cells in dental research.

Authors:  Thekkeparambil Chandrabose Srijaya; Padmaja Jayaprasad Pradeep; Rosnah Binti Zain; Sabri Musa; Noor Hayaty Abu Kasim; Vijayendran Govindasamy
Journal:  Stem Cells Int       Date:  2012-05-09       Impact factor: 5.443

Review 2.  Delayed Eruption of Permanent Dentition and Maxillary Contraction in Patients with Cleidocranial Dysplasia: Review and Report of a Family.

Authors:  A Impellizzeri; G Midulla; U Romeo; C La Monaca; E Barbato; G Galluccio
Journal:  Int J Dent       Date:  2018-07-04

3.  Shaping modern human skull through epigenetic, transcriptional and post-transcriptional regulation of the RUNX2 master bone gene.

Authors:  Lorena Di Pietro; Marta Barba; Daniela Palacios; Federica Tiberio; Chiara Prampolini; Mirko Baranzini; Ornella Parolini; Alessandro Arcovito; Wanda Lattanzi
Journal:  Sci Rep       Date:  2021-10-29       Impact factor: 4.379

4.  Identification of RUNX2 variants associated with cleidocranial dysplasia.

Authors:  Xueren Gao; Kunxia Li; Yanjie Fan; Yu Sun; Xiaomei Luo; Lili Wang; Huili Liu; Zhuwen Gong; Jianguo Wang; Yu Wang; Xuefan Gu; Yongguo Yu
Journal:  Hereditas       Date:  2019-09-16       Impact factor: 3.271

  4 in total

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