Literature DB >> 21530964

Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.

Melanie E Ochalski1, Natalie Engle, Anthony Wakim, Britt J Ravnan, Lori Hoffner, Aleksandar Rajkovic, Urvashi Surti.   

Abstract

OBJECTIVE: To investigate candidate genes affected by a complex X chromosome rearrangement that may play a role in the diagnosis of spontaneous premature ovarian insufficiency (POI).
DESIGN: Prospective cytogenetic analysis, fluorescence in situ hybridization (FISH) analysis and oligonucleotide array comparative genome hybridization (CGH).
SETTING: University medical center. PATIENT(S): A 36-year-old woman with POI found to have a highly rearrangement X chromosome. INTERVENTION(S): FISH analysis and oligonucleotide array CGH. MAIN OUTCOME MEASURE(S): Oligonucleotide microarray analysis to detect duplicated, deleted, or translocated regions of the X chromosome. RESULT(S): Complex rearrangement of the X chromosome involving ≥12 breakpoints resulting in two deletions, four duplications, and several intrachromosomal translocations. At least 13 genes with possible relevance to POI may be affected by the rearrangement. CONCLUSION(S): Array CGH can reveal candidate genes that may have essential roles in fertility and POI.
Copyright © 2011 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21530964     DOI: 10.1016/j.fertnstert.2011.03.082

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  1 in total

1.  Complex X chromosome rearrangement associated with multiorgan autoimmunity.

Authors:  Irén Haltrich; Henriett Pikó; Horolma Pamjav; Anikó Somogyi; Antónia Völgyi; Dezső David; Artúr Beke; Zoltán Garamvölgyi; Eszter Kiss; Veronika Karcagi; György Fekete
Journal:  Mol Cytogenet       Date:  2015-07-19       Impact factor: 2.009

  1 in total

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