Literature DB >> 12807958

Telomeres: a diagnosis at the end of the chromosomes.

B B A De Vries1, R Winter, A Schinzel, C van Ravenswaaij-Arts.   

Abstract

In recent years, subtelomeric rearrangements have been identified as a major cause of mental retardation and/or malformation syndromes. So far, over 2500 subjects with mental retardation have been tested and reported of whom approximately 5% appeared to have a subtelomeric rearrangement. In this review, the clinical aspects of each known (submicroscopic) subtelomeric deletion will be presented and the various methods available for detecting subtelomeric abnormalities will be discussed. Not only will the patients and their families benefit from a good collection and report of the various telomeric abnormalities and their clinical phenotype, but it will also give more insight into the aetiology of mental retardation and malformation syndromes.

Entities:  

Mesh:

Year:  2003        PMID: 12807958      PMCID: PMC1735506          DOI: 10.1136/jmg.40.6.385

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  154 in total

1.  Measurement of locus copy number by hybridisation with amplifiable probes.

Authors:  J A Armour; C Sismani; P C Patsalis; G Cross
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

2.  A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome.

Authors:  D Tentler; P Gustavsson; G Elinder; O Eklöf; L Gordon; A Mandel; N Dahl
Journal:  J Med Genet       Date:  2000-02       Impact factor: 6.318

3.  Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14).

Authors:  B B de Vries; B H Eussen; O P van Diggelen; A van Der Heide; W H Deelen; L C Govaerts; D Lindhout; C H Wouters; J O Van Hemel
Journal:  Am J Med Genet       Date:  1999-11-19

4.  Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).

Authors:  E Holinski-Feder; E Reyniers; S Uhrig; A Golla; J Wauters; P Kroisel; P Bossuyt; I Rost; K Jedele; H Zierler; S Schwab; D Wildenauer; M R Speicher; P J Willems; T Meitinger; R F Kooy
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

Review 5.  11q- syndrome: three cases and a review of the literature.

Authors:  B Leegte; W S Kerstjens-Frederikse; K Deelstra; J H Begeer; A J van Essen
Journal:  Genet Couns       Date:  1999

6.  Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two families.

Authors:  J Wang; L Spitz; R Hayward; E Kiely; C M Hall; D P O'Donoghue; R Palmer; F R Goodman; P J Scambler; R M Winter; W Reardon
Journal:  Eur J Pediatr       Date:  1999-11       Impact factor: 3.183

7.  The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome.

Authors:  D Pfeifer; F Poulat; E Holinski-Feder; F Kooy; G Scherer
Journal:  Genomics       Date:  2000-01-01       Impact factor: 5.736

8.  Subtle chromosomal rearrangements in children with unexplained mental retardation.

Authors:  S J Knight; R Regan; A Nicod; S W Horsley; L Kearney; T Homfray; R M Winter; P Bolton; J Flint
Journal:  Lancet       Date:  1999-11-13       Impact factor: 79.321

9.  Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation.

Authors:  M Rio; F Molinari; S Heuertz; C Ozilou; P Gosset; O Raoul; V Cormier-Daire; J Amiel; S Lyonnet; M Le Merrer; C Turleau; M-C de Blois; M Prieur; S Romana; M Vekemans; A Munnich; L Colleaux
Journal:  J Med Genet       Date:  2002-04       Impact factor: 6.318

10.  High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization.

Authors:  Joris A Veltman; Eric F P M Schoenmakers; Bert H Eussen; Irene Janssen; Gerard Merkx; Brigitte van Cleef; Conny M van Ravenswaaij; Han G Brunner; Dominique Smeets; Ad Geurts van Kessel
Journal:  Am J Hum Genet       Date:  2002-04-09       Impact factor: 11.025

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  46 in total

1.  Microarray analysis of cell-free fetal DNA in amniotic fluid: a prenatal molecular karyotype.

Authors:  Paige B Larrabee; Kirby L Johnson; Ekaterina Pestova; Madhuri Lucas; Kim Wilber; Erik S LeShane; Umadevi Tantravahi; Janet M Cowan; Diana W Bianchi
Journal:  Am J Hum Genet       Date:  2004-07-13       Impact factor: 11.025

2.  Genomic imbalances in mental retardation.

Authors:  M Kriek; S J White; M C Bouma; H G Dauwerse; K B M Hansson; J V Nijhuis; B Bakker; G-J B van Ommen; J T den Dunnen; M H Breuning
Journal:  J Med Genet       Date:  2004-04       Impact factor: 6.318

3.  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

4.  A subtelomeric translocation apparently implied in multiple abortions.

Authors:  Sandra Monfort; Francisco Martínez; Mónica Roselló; Lourdes Badia; Félix Prieto; Carmen Orellana
Journal:  J Assist Reprod Genet       Date:  2006-04-05       Impact factor: 3.412

Review 5.  Investigation of global developmental delay.

Authors:  L McDonald; A Rennie; J Tolmie; P Galloway; R McWilliam
Journal:  Arch Dis Child       Date:  2006-08       Impact factor: 3.791

Review 6.  Balanced translocations in mental retardation.

Authors:  Geert Vandeweyer; R Frank Kooy
Journal:  Hum Genet       Date:  2009-04-05       Impact factor: 4.132

7.  Duplication of the Miller-Dieker Critical Region in a Patient with a Subtelomeric Unbalanced Translocation t(10;17)(p15.3;p13.3).

Authors:  R Ruiz Esparza-Garrido; A C Velázquez-Wong; M A Araujo-Solís; J C Huicochea-Montiel; M Á Velázquez-Flores; F Salamanca-Gómez; D J Arenas-Aranda
Journal:  Mol Syndromol       Date:  2012-07-10

Review 8.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

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

9.  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

10.  A 1-Mb critical region in six patients with 9q34.3 terminal deletion syndrome.

Authors:  Naoki Harada; Remco Visser; Angie Dawson; Makoto Fukamachi; Mie Iwakoshi; Nobuhiko Okamoto; Tatsuya Kishino; Norio Niikawa; Naomichi Matsumoto
Journal:  J Hum Genet       Date:  2004-07-16       Impact factor: 3.172

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