Literature DB >> 22544656

Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by FISH and array-CGH.

Chiara Donatella Viaggi1, Simona Cavani, Mauro Pierluigi, Vincenzo Antona, Ettore Piro, Giovanni Corsello, Massimo Mogni, Maria Piccione, Michela Malacarne.   

Abstract

Complex chromosomal rearrangements (CCRs) are structural aberrations involving more than two chromosomes with at least three breakpoints. CCRs can be divided into familial and de novo. Balanced CCR are extremely rare in humans and are at high risk of producing unbalanced gametes. Individuals with balanced CCR are usually phenotipically normal but report fertility problems, recurrent miscarriages or congenital anomalies in newborn offsprings as consequence of either meiotic failure or imbalanced chromosomes segregation.We describe the case of an unbalanced CCR involving chromosomes 1, 4 and 8 found in a girl with developmental delay, hexadactilia and microcephaly. The rearrangement, apparently balanced at a standard karyotype analysis and of maternal origin, was demonstrated to be unbalanced by array-CGH and FISH. In conclusion our study underlines the importance of the combined use of a quantitative technique, as array-CGH, to detect criptic segmental aneuploidies, and a qualitative tool, as FISH analysis, to physically map the localization of the chromosome segments involved, in order to realize the exact nature that underlies a chromosomal rearrangement.

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Year:  2012        PMID: 22544656     DOI: 10.1007/s13353-012-0097-x

Source DB:  PubMed          Journal:  J Appl Genet        ISSN: 1234-1983            Impact factor:   3.240


  9 in total

1.  Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.

Authors:  B Röthlisberger; D Kotzot; L Brecevic; M Koehler; D Balmer; F Binkert; A Schinzel
Journal:  Eur J Hum Genet       Date:  1999-12       Impact factor: 4.246

2.  Fluorescence in situ hybridization characterization of apparently balanced translocation reveals cryptic complex chromosomal rearrangements with unexpected level of complexity.

Authors:  Philippos C Patsalis; Paola Evangelidou; Spyros Charalambous; Carolina Sismani
Journal:  Eur J Hum Genet       Date:  2004-08       Impact factor: 4.246

Review 3.  The Wnt signaling pathway in development and disease.

Authors:  Catriona Y Logan; Roel Nusse
Journal:  Annu Rev Cell Dev Biol       Date:  2004       Impact factor: 13.827

4.  An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.

Authors:  Iris Bartels; Heike Starke; Loukas Argyriou; Simone M Sauter; Barbara Zoll; Thomas Liehr
Journal:  Eur J Med Genet       Date:  2006-11-10       Impact factor: 2.708

5.  Array CGH detection of a cryptic deletion in a complex chromosome rearrangement.

Authors:  Carla Rosenberg; Jeroen Knijnenburg; Maria de Lourdes Chauffaille; Decio Brunoni; Ana Lucia Catelani; Willem Sloos; Károly Szuhai; Hans J Tanke
Journal:  Hum Genet       Date:  2005-02-22       Impact factor: 4.132

Review 6.  The ups and downs of Wnt signaling in prevalent neurological disorders.

Authors:  G V De Ferrari; R T Moon
Journal:  Oncogene       Date:  2006-12-04       Impact factor: 9.867

7.  Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement.

Authors:  Peining Li; Hui Z Zhang; Shannon Huff; Manjunath Nimmakayalu; Mazin Qumsiyeh; Jingwei Yu; Anna Szekely; Tian Xu; Barbara R Pober
Journal:  Am J Med Genet A       Date:  2006-12-15       Impact factor: 2.802

8.  Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.

Authors:  Houda Karmous-Benailly; Fabienne Giuliano; Christophe Massol; Catherine Bloch; Dominique De Ricaud; Jean-Claude Lambert; Serge Perelman
Journal:  Eur J Med Genet       Date:  2006-02-10       Impact factor: 2.708

9.  Syntabulin-kinesin-1 family member 5B-mediated axonal transport contributes to activity-dependent presynaptic assembly.

Authors:  Qian Cai; Ping-Yue Pan; Zu-Hang Sheng
Journal:  J Neurosci       Date:  2007-07-04       Impact factor: 6.167

  9 in total
  1 in total

1.  NF1 microdeletion syndrome: case report of two new patients.

Authors:  Gregorio Serra; Vincenzo Antona; Giovanni Corsello; Federico Zara; Ettore Piro; Raffaele Falsaperla
Journal:  Ital J Pediatr       Date:  2019-11-08       Impact factor: 2.638

  1 in total

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