Literature DB >> 11702226

Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH.

C A Joyce1, N R Dennis, S Cooper, C E Browne.   

Abstract

The cause of mental retardation, present in approximately 3% of the population, is unexplained in the majority of cases. Recent reports have suggested that cryptic telomeric rearrangements resulting in segmental aneuploidy and gene-dosage imbalance might represent a significant cause of idiopathic mental retardation (IMR). Two groups of patients with unexplained developmental delay (unselected and selected) and a group of control individuals have been investigated to determine the frequency of submicroscopic telomeric rearrangements associated with IMR and the frequency within the normal population. In contrast to current thinking, our data have shown that true cryptic telomeric rearrangements are not a significant cause of IMR. No fully cryptic abnormalities were detected in our IMR groups, although a semi-cryptic unbalanced telomeric translocation was identified in one selected patient by high-resolution G-band analysis. This abnormality was confirmed and characterised by fluorescence in situ hybridisation (FISH) with telomere-specific probes. A further 13 cytogenetically detected subtle terminal rearrangements were characterised by using multi-telomere FISH. Seven of these had previously been reported as normal, three of which were shown to be interstitial deletions. These cases illustrate the importance of high-resolution analysis to exclude subtle but cytogenetically visible abnormalities prior to subtelomere FISH screening when determining the frequency of cryptic telomeric rearrangements. Unexpectedly, two cryptic telomeric abnormalities were detected among our control individuals, suggesting that submicroscopic telomeric abnormalities may be a not uncommon finding in the general population. Hence, our data have important implications when defining the significance of cryptic telomeric rearrangements detected during screening programmes.

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Mesh:

Year:  2001        PMID: 11702226     DOI: 10.1007/s004390100588

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  23 in total

Review 1.  Telomeres: a diagnosis at the end of the chromosomes.

Authors:  B B A De Vries; R Winter; A Schinzel; C van Ravenswaaij-Arts
Journal:  J Med Genet       Date:  2003-06       Impact factor: 6.318

2.  Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.

Authors:  J B Ravnan; J H Tepperberg; P Papenhausen; A N Lamb; J Hedrick; D Eash; D H Ledbetter; C L Martin
Journal:  J Med Genet       Date:  2005-09-30       Impact factor: 6.318

3.  High throughput screening of human subtelomeric DNA for copy number changes using multiplex amplifiable probe hybridisation (MAPH).

Authors:  E J Hollox; T Atia; G Cross; T Parkin; J A L Armour
Journal:  J Med Genet       Date:  2002-11       Impact factor: 6.318

4.  Subtelomeric rearrangements in idiopathic mental retardation.

Authors:  Gopalrao V N Velagaleti; Sally S Robinson; Bobby M Rouse; Vijay S Tonk; Lillian H Lockhart
Journal:  Indian J Pediatr       Date:  2005-08       Impact factor: 1.967

5.  A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities.

Authors:  Annette E Cockwell; Patricia A Jacobs; Sarah J Beal; John A Crolla
Journal:  Hum Genet       Date:  2003-01-08       Impact factor: 4.132

6.  Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience.

Authors:  C D M van Karnebeek; C Koevoets; S Sluijter; E K Bijlsma; D F M C Smeets; E J Redeker; R C M Hennekam; J M N Hoovers
Journal:  J Med Genet       Date:  2002-08       Impact factor: 6.318

7.  To determine the frequency of subtelomeric abnormalities in children with idiopathic mental retardation.

Authors:  K S Rana; R G Holla
Journal:  Med J Armed Forces India       Date:  2011-10-22

8.  Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms.

Authors:  H L Wilson; A C C Wong; S R Shaw; W-Y Tse; G A Stapleton; M C Phelan; S Hu; J Marshall; H E McDermid
Journal:  J Med Genet       Date:  2003-08       Impact factor: 6.318

9.  "Molecular rulers" for calibrating phenotypic effects of telomere imbalance.

Authors:  C L Martin; D J Waggoner; A Wong; S Uhrig; J A Roseberry; J F Hedrick; S D Pack; K Russell; E Zackai; W B Dobyns; D H Ledbetter
Journal:  J Med Genet       Date:  2002-10       Impact factor: 6.318

10.  Two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20.

Authors:  Cheryl Descipio; Jennifer D Morrissette; Laura K Conlin; Dinah Clark; Maninder Kaur; James Coplan; Harold Riethman; Nancy B Spinner; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2010-02       Impact factor: 2.802

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