Literature DB >> 11005146

Telomere-telomere (end to end) fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2-->p15.1: phenotypic consequences and possible mechanisms.

S M Zneimer1, P D Cotter, S D Stewart.   

Abstract

We report a rare case of a de novo end to end fusion of chromosomes 7 and 22 in conjunction with an interstitial deletion of chromosome 7p11.2p15.1 in a newborn with congenital anomalies. The proband presented for chromosome analysis with bilateral cataracts, dysmorphic facies and distal limb abnormalities. Chromosome analysis showed a 45,XY,der(22)psu dic(22;7)(p13;p22.3)del(7)(p11.2p15.1) karyotype. This short arm to short arm fusion of chromosomes 7 and 22 resulted in a pseudodicentric chromosome. The interstitial deletion in the short arm of chromosome 7 was likely a result of breakage and reunion related to instability of the dicentric chromosome. Loss of genetic material in this region of chromosome 7p has been implicated in the pathophysiology of craniosynostosis and cephalopolysyndactyly syndromes.

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Year:  2000        PMID: 11005146     DOI: 10.1034/j.1399-0004.2000.580207.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  7 in total

1.  Risk evaluation and preimplantation genetic diagnosis in an infertile man with an unbalanced translocation t(10;15) resulting in a healthy baby.

Authors:  De-Hua Cheng; Fei Gong; Chang-Fu Lu; Lu-Yun Li; Guang-Xiu Lu; Yue-Qiu Tan
Journal:  J Assist Reprod Genet       Date:  2012-09-22       Impact factor: 3.412

2.  Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.

Authors:  Zafer Cetin; Mesut Parlak; Ozden Altiok Clark; Gungor Karaguzel; Guven Luleci; Iffet Bircan; Sibel Berker-Karauzum
Journal:  Eur J Pediatr       Date:  2013-05-08       Impact factor: 3.183

Review 3.  Genetic advances in craniosynostosis.

Authors:  Wanda Lattanzi; Marta Barba; Lorena Di Pietro; Simeon A Boyadjiev
Journal:  Am J Med Genet A       Date:  2017-02-04       Impact factor: 2.802

4.  Greig cephalopolysyndactyly (GCPS) contiguous gene syndrome in a boy with a 14 Mb deletion in region 7p13-14 caused by a paternal balanced insertion (5; 7).

Authors:  Solveig Schulz; Marianne Volleth; Petra Muschke; Ilse Wieland; Peter Wieacker
Journal:  Appl Clin Genet       Date:  2008-11-18

5.  A 9p13-->p24 duplication coupled with a whole 22q translocation onto 9p24.

Authors:  Horacio Rivera; Ana I Vásquez-Velásquez; Mariá de Lourdes Ramirez-Duenas; Luis Eduardo Becerra-Solano
Journal:  J Appl Genet       Date:  2007       Impact factor: 2.653

6.  Clinical, cytogenetic and molecular genetic characterization of a tandem fusion translocation in a male Holstein cattle with congenital hypospadias and a ventricular septal defect.

Authors:  Alessandra Iannuzzi; Marina Braun; Viviana Genualdo; Angela Perucatti; Sina Reinartz; Ioannis Proios; Maike Heppelmann; Jürgen Rehage; Kirsten Hülskötter; Andreas Beineke; Julia Metzger; Ottmar Distl
Journal:  PLoS One       Date:  2020-01-10       Impact factor: 3.240

Review 7.  Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.

Authors:  Kinga Kozma; Marius Bembea; Claudia M Jurca; Mihai Ioana; Ioana Streață; Simona Ş Şoşoi; Andrei Pirvu; Codruța D Petchesi; Ariana Szilágyi; Cristian N Sava; Alexandru Jurca; Anikó Ujfalusi; Zsuzsanna Szűcs; Katalin Szakszon
Journal:  Genes (Basel)       Date:  2021-10-23       Impact factor: 4.096

  7 in total

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