Literature DB >> 18663743

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.

Lina Shao1, Chad A Shaw, Xin-Yan Lu, Trilochan Sahoo, Carlos A Bacino, Seema R Lalani, Pawel Stankiewicz, Svetlana A Yatsenko, Yinfeng Li, Sarah Neill, Amber N Pursley, A Craig Chinault, Ankita Patel, Arthur L Beaudet, James R Lupski, Sau W Cheung.   

Abstract

Subtelomeric imbalances are a significant cause of congenital disorders. Screening for these abnormalities has traditionally utilized GTG-banding analysis, fluorescence in situ hybridization (FISH) assays, and multiplex ligation-dependent probe amplification. Microarray-based comparative genomic hybridization (array-CGH) is a relatively new technology that can identify microscopic and submicroscopic chromosomal imbalances. It has been proposed that an array with extended coverage at subtelomeric regions could characterize subtelomeric aberrations more efficiently in a single experiment. The targeted arrays for chromosome microarray analysis (CMA), developed by Baylor College of Medicine, have on average 12 BAC/PAC clones covering 10 Mb of each of the 41 subtelomeric regions. We screened 5,380 consecutive clinical patients using CMA. The most common reasons for referral included developmental delay (DD), and/or mental retardation (MR), dysmorphic features (DF), multiple congenital anomalies (MCA), seizure disorders (SD), and autistic, or other behavioral abnormalities. We found pathogenic rearrangements at subtelomeric regions in 236 patients (4.4%). Among these patients, 103 had a deletion, 58 had a duplication, 44 had an unbalanced translocation, and 31 had a complex rearrangement. The detection rates varied among patients with a normal karyotype analysis (2.98%), with an abnormal karyotype analysis (43.4%), and with an unavailable or no karyotype analysis (3.16%). Six patients out of 278 with a prior normal subtelomere-FISH analysis showed an abnormality including an interstitial deletion, two terminal deletions, two interstitial duplications, and a terminal duplication. In conclusion, genomic imbalances at subtelomeric regions contribute significantly to congenital disorders. Targeted array-CGH with extended coverage (up to 10 Mb) of subtelomeric regions will enhance the detection of subtelomeric imbalances, especially for submicroscopic imbalances. (c) 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 18663743      PMCID: PMC2680131          DOI: 10.1002/ajmg.a.32399

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


  49 in total

1.  Subtelomeric chromosome aberrations: still a lot to learn.

Authors:  U Moog; Y H J M Arens; J C M van Lent-Albrechts; P E A Huijts; E E J Smeets; C T R M Schrander-Stumpel; J J M Engelen
Journal:  Clin Genet       Date:  2005-11       Impact factor: 4.438

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.  Clinical experience with array CGH: case presentations from nine months of practice.

Authors:  Alexis F Poss; Paula C Goldenberg; Catherine W Rehder; Hutton M Kearney; Elizabeth C Melvin; Dwight D Koeberl; Marie T McDonald
Journal:  Am J Med Genet A       Date:  2006-10-01       Impact factor: 2.802

4.  Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

Authors:  Lisa G Shaffer; Catherine D Kashork; Reza Saleki; Emily Rorem; Kyle Sundin; Blake C Ballif; Bassem A Bejjani
Journal:  J Pediatr       Date:  2006-07       Impact factor: 4.406

Review 5.  Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders.

Authors:  Jennifer A Lee; James R Lupski
Journal:  Neuron       Date:  2006-10-05       Impact factor: 17.173

6.  Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation.

Authors:  Klaas Kok; Trijnie Dijkhuizen; Yolanthe E Swart; Hanny Zorgdrager; Pieter van der Vlies; Rudolf Fehrmann; Gerard J te Meerman; Klasien B J Gerssen-Schoorl; Ton van Essen; Birgit Sikkema-Raddatz; Charles H C M Buys
Journal:  Eur J Med Genet       Date:  2005 Jul-Sep       Impact factor: 2.708

Review 7.  Medical applications of array CGH and the transformation of clinical cytogenetics.

Authors:  L G Shaffer; B A Bejjani
Journal:  Cytogenet Genome Res       Date:  2006       Impact factor: 1.636

8.  Severe expressive-language delay related to duplication of the Williams-Beuren locus.

Authors:  Martin J Somerville; Carolyn B Mervis; Edwin J Young; Eul-Ju Seo; Miguel del Campo; Stephen Bamforth; Ella Peregrine; Wayne Loo; Margaret Lilley; Luis A Pérez-Jurado; Colleen A Morris; Stephen W Scherer; Lucy R Osborne
Journal:  N Engl J Med       Date:  2005-10-20       Impact factor: 91.245

9.  Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.

Authors:  B Menten; N Maas; B Thienpont; K Buysse; J Vandesompele; C Melotte; T de Ravel; S Van Vooren; I Balikova; L Backx; S Janssens; A De Paepe; B De Moor; Y Moreau; P Marynen; J-P Fryns; G Mortier; K Devriendt; F Speleman; J R Vermeesch
Journal:  J Med Genet       Date:  2006-02-20       Impact factor: 6.318

Review 10.  Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes.

Authors:  James R Lupski; Pawel Stankiewicz
Journal:  PLoS Genet       Date:  2005-12       Impact factor: 5.917

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  44 in total

1.  Primed in situ labeling technique for subtelomeric rearrangements in 70 children with idiopathic mental retardation.

Authors:  Hong Tian; Hui Yu; Siqing Fu; Runming Jin
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2011-12-16

2.  Detection of clinically relevant exonic copy-number changes by array CGH.

Authors:  Philip M Boone; Carlos A Bacino; Chad A Shaw; Patricia A Eng; Patricia M Hixson; Amber N Pursley; Sung-Hae L Kang; Yaping Yang; Joanna Wiszniewska; Beata A Nowakowska; Daniela del Gaudio; Zhilian Xia; Gayle Simpson-Patel; LaDonna L Immken; James B Gibson; Anne C-H Tsai; Jennifer A Bowers; Tyler E Reimschisel; Christian P Schaaf; Lorraine Potocki; Fernando Scaglia; Tomasz Gambin; Maciej Sykulski; Magdalena Bartnik; Katarzyna Derwinska; Barbara Wisniowiecka-Kowalnik; Seema R Lalani; Frank J Probst; Weimin Bi; Arthur L Beaudet; Ankita Patel; James R Lupski; Sau Wai Cheung; Pawel Stankiewicz
Journal:  Hum Mutat       Date:  2010-11-02       Impact factor: 4.878

3.  Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalus.

Authors:  Annemieke J M H Verkerk; Rachel Schot; Laura van Waterschoot; Hannie Douben; Pino J Poddighe; Maarten H Lequin; Linda S de Vries; Paulien Terhal; Johanne M D Hahnemann; Irenaeus F M de Coo; Marie-Claire Y de Wit; Leontien S Wafelman; Livia Garavelli; William B Dobyns; Peter J Van der Spek; Annelies de Klein; Grazia M S Mancini
Journal:  Am J Med Genet A       Date:  2010-06       Impact factor: 2.802

4.  Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.

Authors:  Svetlana A Yatsenko; Ellen K Brundage; Erin K Roney; Sau Wai Cheung; A Craig Chinault; James R Lupski
Journal:  Hum Mol Genet       Date:  2009-03-17       Impact factor: 6.150

5.  Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.

Authors:  Pengfei Liu; Ayelet Erez; Sandesh C Sreenath Nagamani; Weimin Bi; Claudia M B Carvalho; Alexandra D Simmons; Joanna Wiszniewska; Ping Fang; Patricia A Eng; M Lance Cooper; V Reid Sutton; Elizabeth R Roeder; John B Bodensteiner; Mauricio R Delgado; Siddharth K Prakash; John W Belmont; Pawel Stankiewicz; Jonathan S Berg; Marwan Shinawi; Ankita Patel; Sau Wai Cheung; James R Lupski
Journal:  Hum Mol Genet       Date:  2011-02-25       Impact factor: 6.150

6.  Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements.

Authors:  Yue Luo; Karen E Hermetz; Jodi M Jackson; Jennifer G Mulle; Anne Dodd; Karen D Tsuchiya; Blake C Ballif; Lisa G Shaffer; Jannine D Cody; David H Ledbetter; Christa L Martin; M Katharine Rudd
Journal:  Hum Mol Genet       Date:  2011-07-04       Impact factor: 6.150

7.  "Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements.

Authors:  Maryam Rafati; Mohammad R Ghadirzadeh; Yaser Heshmati; Homeira Adibi; Zarrintaj Keihanidoust; Mohammad R Eshraghian; Jila Dastan; Azadeh Hoseini; Marzieh Purhoseini; Saeed R Ghaffari
Journal:  Mol Cytogenet       Date:  2012-01-19       Impact factor: 2.009

8.  Use of Multiplex Ligation-Dependent Probe Amplification (MLPA) in screening of subtelomeric regions in children with idiopathic mental retardation.

Authors:  Kausik Mandal; Vijay R Boggula; Minal Borkar; Suraksha Agarwal; Shubha R Phadke
Journal:  Indian J Pediatr       Date:  2009-11-12       Impact factor: 1.967

9.  Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation.

Authors:  Ye Wu; Taoyun Ji; Jingmin Wang; Jing Xiao; Huifang Wang; Jie Li; Zhijie Gao; Yanling Yang; Bin Cai; Liwen Wang; Zhongshu Zhou; Lili Tian; Xiaozhu Wang; Nan Zhong; Jiong Qin; Xiru Wu; Yuwu Jiang
Journal:  BMC Med Genet       Date:  2010-05-11       Impact factor: 2.103

Review 10.  Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature.

Authors:  Michael R Rossi; Miriam S DiMaio; Bixia Xiang; Kangmo Lu; Hande Kaymakcalan; Margretta Seashore; Maurice J Mahoney; Peining Li
Journal:  Am J Med Genet A       Date:  2009-12       Impact factor: 2.802

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