Literature DB >> 15108196

Prospective study comparing HR-CGH and subtelomeric FISH for investigation of individuals with mental retardation and dysmorphic features and an update of a study using only HR-CGH.

Maria Kirchhoff1, Søren Pedersen, Eigil Kjeldsen, Hanne Rose, Morten Dunø, Steen Kølvraa, Claes Lundsteen.   

Abstract

In a prospective study 94 individuals with mental retardation (MR) and dysmorphic features with normal conventional karyotypes were investigated by both subtelomeric FISH and high resolution CGH (HR-CGH) in order to compare the potential of the two techniques in this application. A total of 9.6% abnormalities were found with HR-CGH and subtelomeric FISH, with HR-CGH detecting 8.5% (95% CI: 4.4-15.9) and FISH 3.2% (95% CI: 1.2-9.0). Thus, the techniques complemented each other, however, the diagnostic yield appeared higher of HR-CGH than of subtelomeric FISH, as most aberrations were interstitial. Another 330 individuals with MR and dysmorphic features with normal conventional karyotypes were investigated by HR-CGH on a routine basis. When added to the analyses of the prospective study a total of 51/424 (12%; 95% CI: 9.3-15.5) abnormalities were found, of which the majority were interstitial. We conclude that HR-CGH is well suited for routine screening for cryptic chromosomal imbalances in patients with MR and dysmorphic features. It is likely that the use of the technique in this application will reinforce the effort of defining new syndromes. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15108196     DOI: 10.1002/ajmg.a.20678

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 in total

1.  Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

Authors:  L Rickman; H Fiegler; C Shaw-Smith; R Nash; V Cirigliano; G Voglino; B L Ng; C Scott; J Whittaker; M Adinolfi; N P Carter; M Bobrow
Journal:  J Med Genet       Date:  2005-09-30       Impact factor: 6.318

2.  Subtelomeric chromosome rearrangements in children with idiopathic mental retardation: applicability of three molecular-cytogenetic methods.

Authors:  Alenka Erjavec-Skerget; Spela Stangler-Herodez; Andreja Zagorac; Boris Zagradisnik; Nadja Kokalj-Vokac
Journal:  Croat Med J       Date:  2006-12       Impact factor: 1.351

Review 3.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

4.  Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion.

Authors:  Morten Dunø; Hanne Hove; Maria Kirchhoff; Koenraad Devriendt; Marianne Schwartz
Journal:  Hum Genet       Date:  2004-09-18       Impact factor: 4.132

5.  Selection of cell-type specific antibodies on tissue-sections using phage display.

Authors:  Simon Asbjørn Larsen; Theresa Meldgaard; Simon Lykkemark; Ole Aalund Mandrup; Peter Kristensen
Journal:  J Cell Mol Med       Date:  2015-03-26       Impact factor: 5.310

6.  Screening for Subtelomeric Rearrangements in Thai Patients with Intellectual Disabilities Using FISH and Review of Literature on Subtelomeric FISH in 15,591 Cases with Intellectual Disabilities.

Authors:  Chariyawan Charalsawadi; Jariya Khayman; Verayuth Praphanphoj; Pornprot Limprasert
Journal:  Genet Res Int       Date:  2016-10-16
  6 in total

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