Literature DB >> 27022331

Partial 1q Duplications and Associated Phenotype.

Marcos L M Morris1, José E Baroneza2, Patricia Teixeira1, Cristina T N Medina3, Mara S Cordoba3, Beatriz R Versiani3, Liege L Roese4, Erika L Freitas5, Ana C S Fonseca5, Maria C G Dos Santos6, Aline Pic-Taylor7, Carla Rosenberg5, Silviene F Oliveira7, Iris Ferrari8, Juliana F Mazzeu9.   

Abstract

Duplications of the long arm of chromosome 1 are rare. Distal duplications are the most common and have been reported as either pure trisomy or unbalanced translocations. The paucity of cases with pure distal 1q duplications has made it difficult to delineate a partial distal trisomy 1q syndrome. Here, we report 2 patients with overlapping 1q duplications detected by G-banding. Array CGH and FISH were performed to characterize the duplicated segments, exclude the involvement of other chromosomes and determine the orientation of the duplication. Patient 1 presents with a mild phenotype and carries a 22.5-Mb 1q41q43 duplication. Patient 2 presents with a pure 1q42.13qter inverted duplication of 21.5 Mb, one of the smallest distal 1q duplications ever described and one of the few cases characterized by array CGH, thus contributing to a better characterization of distal 1q duplication syndrome.

Entities:  

Keywords:  Array CGH; Distal partial duplication 1q; Duplication 1q41q43; Duplication 1q42.13; FISH

Year:  2016        PMID: 27022331      PMCID: PMC4803000          DOI: 10.1159/000443599

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  31 in total

1.  Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.

Authors:  Yalçin Kímya; Tahsin Yakut; Unal Egelí; Kemal Ozerkan
Journal:  Prenat Diagn       Date:  2002-11       Impact factor: 3.050

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

Authors:  A Polityko; H Starke; N Rumyantseva; U Claussen; T Liehr; S Raskin
Journal:  Cytogenet Genome Res       Date:  2005       Impact factor: 1.636

3.  Wnt signaling acts and is regulated in a human osteoblast differentiation dependent manner.

Authors:  M Eijken; I M J Meijer; I Westbroek; M Koedam; H Chiba; A G Uitterlinden; H A P Pols; J P T M van Leeuwen
Journal:  J Cell Biochem       Date:  2008-05-15       Impact factor: 4.429

Review 4.  Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndrome.

Authors:  W Emberger; E Petek; P M Kroisel; H Zierler; K Wagner
Journal:  Am J Med Genet       Date:  2001-12-15

5.  Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome.

Authors:  J F Mazzeu; A M Vianna-Morgante; A C V Krepischi; A Oudakker; C Rosenberg; K Szuhai; J McGill; J Maccraughan; H van Bokhoven; H G Brunner
Journal:  Clin Genet       Date:  2010-01-20       Impact factor: 4.438

6.  Differential activation of canonical Wnt signaling determines cranial sutures fate: a novel mechanism for sagittal suture craniosynostosis.

Authors:  Björn Behr; Michael T Longaker; Natalina Quarto
Journal:  Dev Biol       Date:  2010-06-12       Impact factor: 3.582

Review 7.  The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.

Authors:  Lisa G Shaffer; Aaron Theisen; Bassem A Bejjani; Blake C Ballif; Arthur S Aylsworth; Cynthia Lim; Marie McDonald; Jay W Ellison; Dana Kostiner; Sulagna Saitta; Tamim Shaikh
Journal:  Genet Med       Date:  2007-09       Impact factor: 8.822

8.  Glucocorticoid-dependent Wnt signaling by mature osteoblasts is a key regulator of cranial skeletal development in mice.

Authors:  Hong Zhou; Wendy Mak; Robert Kalak; Janine Street; Colette Fong-Yee; Yu Zheng; Colin R Dunstan; Markus J Seibel
Journal:  Development       Date:  2009-02       Impact factor: 6.868

9.  Congenital ocular defects associated with an abnormality of the human chromosome 1: trisomy 1q32-qter.

Authors:  B J Clark; G W Lowther; W R Lee
Journal:  J Pediatr Ophthalmol Strabismus       Date:  1994 Jan-Feb       Impact factor: 1.402

10.  Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis.

Authors:  Heather C Mefford; Neil Shafer; Francesca Antonacci; Jesse M Tsai; Sarah S Park; Anne V Hing; Mark J Rieder; Matthew D Smyth; Matthew L Speltz; Evan E Eichler; Michael L Cunningham
Journal:  Am J Med Genet A       Date:  2010-09       Impact factor: 2.802

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  4 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.  [Genetic analysis of a fetus with multiple malformations caused by complex translocations of four chromosomes].

Authors:  Yuqin Luo; Min Shen; Yixi Sun; Yeqing Qian; Liya Wang; Jialing Yu; Junjie Hu; Fan Jin; Minyue Dong
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2019-06-25

3.  An Apparently Balanced Complex Chromosome Rearrangement Involving Seven Breaks and Four Chromosomes in a Healthy Female and Segregation/Recombination in Her Affected Son.

Authors:  Ana Eduarda Campos; Carla Rosenberg; Ana Krepischi; Marina França; Vanessa Lopes; Viviane Nakano; Tânia Vertemati; Marcos Cochak; Michele Migliavacca; Fernanda Milanezi; Ana Cristina Sousa; Juliana Silva; Lígia Vieira; Priscilla Monfredini; Ana Carolina Palumbo; Jonathas Fernandes; Eduardo Perrone
Journal:  Mol Syndromol       Date:  2021-07-15

4.  A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements.

Authors:  Tomohiro Kohmoto; Nana Okamoto; Takuya Naruto; Chie Murata; Yuya Ouchi; Naoko Fujita; Hidehito Inagaki; Shigeko Satomura; Nobuhiko Okamoto; Masako Saito; Kiyoshi Masuda; Hiroki Kurahashi; Issei Imoto
Journal:  Mol Cytogenet       Date:  2017-04-28       Impact factor: 2.009

  4 in total

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