Literature DB >> 26318482

De novo double reciprocal translocations in addition to partial monosomy at another chromosome: A very rare case.

Milena Simioni1, Carlos Eduardo Steiner1, Vera Lúcia Gil-da-Silva-Lopes2.   

Abstract

Reciprocal translocations are one of themost common structural rearrangements with a frequency of 1:500 and occur when there is an exchange of distal segments to breakpoints between non-homologous chromosomes. Two or three independent, simple reciprocal or Robertsonian translocations co-exist in the same carrier were classified as complex chromosome rearrangements (CCRs). Structural chromosome rearrangements are considered balanced when there is no apparent gain or loss of chromosome material. In majority of cases, apparently balanced structural chromosome rearrangements (ABCR) are not associated with abnormal phenotypes, although these have been described in 6% of de novo ABCR and 23% of apparently balanced CCR. Here we report a patient with de novo two apparently balanced reciprocal translocations and two partial monosomies, one of these involving an independent chromosome characterized by microarray. Structural rearrangement investigations can improve the knowledge about human genome architecture and correlation of genomic imbalances to abnormal phenotype.

Entities:  

Keywords:  Apparently balanced chromosome rearrangements; Complex chromosome rearrangements; Microarray; Reciprocal translocation

Mesh:

Year:  2015        PMID: 26318482     DOI: 10.1016/j.gene.2015.08.050

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  3 in total

1.  Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes.

Authors:  Milena Simioni; François Artiguenave; Vincent Meyer; Ilária C Sgardioli; Nilma L Viguetti-Campos; Isabella Lopes Monlleó; Andréa T Maciel-Guerra; Carlos E Steiner; Vera L Gil-da-Silva-Lopes
Journal:  Mol Syndromol       Date:  2017-06-01

2.  Inheritance of a Balanced t(12;20)(q24.33;p12.2) and Unbalanced der(13)t(7;13)(p21.3;q33.2) from a Maternally Derived Double Balanced Translocation Carrier.

Authors:  Jess F Peterson; Gabrielle C Geddes; Donald G Basel; Dana Schippman; John W Grignon; Peter vanTuinen; Ulrike P Kappes
Journal:  J Pediatr Genet       Date:  2017-08-14

3.  Investigation of copy number variations on chromosome 21 detected by comparative genomic hybridization (CGH) microarray in patients with congenital anomalies.

Authors:  Wenfu Li; Xianfu Wang; Shibo Li
Journal:  Mol Cytogenet       Date:  2018-08-10       Impact factor: 2.009

  3 in total

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