Literature DB >> 15750018

A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection.

Alma Kuechler1, Monika Ziegler, Cornelia Blank, Birgit Rommel, Joern Bullerdiek, Jochen Ahrens, Uwe Claussen, Thomas Liehr.   

Abstract

We report a case of a de novo complex chromosomal rearrangement among five chromosomes found in a clinically healthy woman. The only indication for chromosome analysis was a planned intracytoplasmatic sperm injection. Physical examination, including internal and external genitals, and ovaries and hormone status were normal. Banding cytogenetics showed a rearrangement among chromosomes #3, #4, #7, #9, and #17. Twenty-four-color fluorescence in situ hybridization and multicolor banding were applied to characterize the translocations and breakpoints more precisely. This confirmed the involved chromosomes and revealed two breakpoints in chromosome #4. This six-breakpoint rearrangement [der(3)t(3;4), der(4)t(17;4;7), der(7)t(3;7), der(9)t(4;9), and der(17)t(9;17)] seemed to be balanced on a molecular cytogenetic level, although submicroscopic deletions or duplications close to the breakpoints cannot be excluded.

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Year:  2005        PMID: 15750018     DOI: 10.1369/jhc.4B6437.2005

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  5 in total

1.  A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.

Authors:  Natalia Trpchevska; Ivanka Dimova; Tatyana Arabadji; Tanya Milachich; Svetlana Angelova; Magdalena Dimitrova; Mariela Hristova-Savova; Petya Andreeva; Tania Timeva; Atanas Shterev
Journal:  J Assist Reprod Genet       Date:  2017-02-24       Impact factor: 3.412

Review 2.  Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements.

Authors:  Martin Poot; Thomas Haaf
Journal:  Mol Syndromol       Date:  2015-08-15

3.  Exceptional complex chromosomal rearrangements in three generations.

Authors:  Hannie Kartapradja; Nanis Sacharina Marzuki; Mark D Pertile; David Francis; Lita Putri Suciati; Helena Woro Anggaratri; Debby Dwi Ambarwati; Firman Prathama Idris; Harry Lesmana; Hidayat Trimarsanto; Chrysantine Paramayuda; Alida Roswita Harahap
Journal:  Case Rep Genet       Date:  2015-02-03

4.  Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies.

Authors:  L E L M Vissers; P Stankiewicz; S A Yatsenko; E Crawford; H Creswick; V K Proud; B B A de Vries; R Pfundt; C L M Marcelis; J Zackowski; W Bi; A Geurts van Kessel; J R Lupski; J A Veltman
Journal:  Hum Genet       Date:  2007-04-25       Impact factor: 4.132

5.  The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2.

Authors:  Lusine Nazaryan; Eunice G Stefanou; Claus Hansen; Nadezda Kosyakova; Mads Bak; Freddie H Sharkey; Theodora Mantziou; Anastasios D Papanastasiou; Voula Velissariou; Thomas Liehr; Maria Syrrou; Niels Tommerup
Journal:  Eur J Hum Genet       Date:  2013-07-17       Impact factor: 4.246

  5 in total

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