Unusual 8p inverted duplication deletion with telomere capture from 8q

被引:25
|
作者
Buysse, Karen [1 ]
Antonacci, Francesca [2 ]
Callewaert, Bert [1 ]
Loeys, Bart [1 ]
Fraenkel, Ulrike [3 ]
Siu, Victoria [4 ]
Mortier, Geert [1 ]
Speleman, Frank [1 ]
Menten, Bjoern [1 ]
机构
[1] Ghent Univ Hosp, Ctr Med Genet, B-9000 Ghent, Belgium
[2] Univ Washington, Howard Hughes Med Inst, Dept Genome Sci, Seattle, WA 98195 USA
[3] Ghent Univ Hosp, Ctr Dev Disorders, B-9000 Ghent, Belgium
[4] Univ Western Ontario, Dept Pediat, Div Med Genet, Schulich Sch Med, London, ON N6A 3K7, Canada
关键词
Inv dup del (8p); Telomere capture; Oligo array CGH; RECEPTOR-GENE CLUSTERS; INVERSION DUPLICATION; TERMINAL DELETIONS; SHORT ARM; CHROMOSOME-8; REARRANGEMENTS; TRANSLOCATION; HYBRIDIZATION; DEFICIENCY; MECHANISMS;
D O I
10.1016/j.ejmg.2008.10.007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Inverted 8p duplication deletions are recurrent chromosomal rearrangements that are mediated through non-allelic homologous recombination (NAHR) between olfactory receptor (OR) gene clusters at 8p23.1. These rearrangements result in a proximal inverted duplication of various extent, a single copy region between the OR gene clusters and a terminal 8p deletion. The terminal deletions are stabilized by direct addition of telomeric repeats, so called telomere healing. Here, we report a patient with an unusual inverted duplication deletion of 8p. Stabilization of the broken chromosome end was achieved by telomere capture instead of telomere healing, resulting in an additional duplication of 8q24.13 -> qter on the short arm of chromosome 8. Moreover, the inverted duplication was only 3.4 Mb in size (restricted to band 8p22) and thus cytogenetically undetectable. To the best of our knowledge this is the smallest inverted duplication reported hitherto. We describe the molecular characterization by FISH and array CGH of this unusual inv dup del (8p) and a previously reported patient with a similar 8q duplication and review the literature on cases associated with telomere capture. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:31 / 36
页数:6
相关论文
共 50 条
  • [41] An unusual case of mosaicism for a cryptic complex inversion duplication 8p and ring (inv dup 8p) demonstrates a novel mechanism of chromosome stabilization.
    Chernos, J
    Innes, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 303 - 303
  • [42] Telomere Capture as a Frequent Mechanism for Stabilization of the Terminal Chromosomal Deletion Associated with Inverted Duplication
    Yu, S.
    Graf, W. D.
    CYTOGENETIC AND GENOME RESEARCH, 2010, 129 (04) : 265 - 274
  • [43] Monocentric, inverted duplication of 8p due to a maternal paracentric inversion: phenotype and proposal of a mechanism.
    Forrester, SR
    Ravnan, JB
    Schneider, MC
    GENETICS IN MEDICINE, 2004, 6 (04) : 320 - 320
  • [44] 8p deletion and 9p duplication in two children with electrical status epilepticus in sleep syndrome
    Nakayama, Tojo
    Nabatame, Shin
    Saito, Yoshiaki
    Nakagawa, Eiji
    Shimojima, Keiko
    Yamamoto, Toshiyuki
    Kaneko, Yu
    Okumura, Keiko
    Fujie, Hiromi
    Uematsu, Mitsugu
    Komaki, Hirofumi
    Sugai, Kenji
    Sasaki, Masayuki
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2012, 21 (04): : 295 - 299
  • [45] Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: Genotype-phenotype correlation for anomalies of the corpus callosum
    Vibert, Roseline
    Mignot, Cyril
    Keren, Boris
    Chantot-Bastaraud, Sandra
    Portnoi, Marie-France
    Nougues, Marie-Christine
    Moutard, Marie-Laure
    Faudet, Anne
    Whalen, Sandra
    Haye, Damien
    Garel, Catherine
    Chatron, Nicolas
    Rossi, Massimiliano
    Vincent-Delorme, Catherine
    Boute, Odile
    Delobel, Bruno
    Andrieux, Joris
    Devillard, Francoise
    Coutton, Charles
    Puechberty, Jacques
    Pebrel-Richard, Celine
    Colson, Cindy
    Gerard, Marion
    Missirian, Chantal
    Sigaudy, Sabine
    Busa, Tiffany
    Doco-Fenzy, Martine
    Malan, Valerie
    Rio, Marlene
    Doray, Berenice
    Sanlaville, Damien
    Siffroi, Jean-Pierre
    Heron, Delphine
    Heide, Solveig
    CLINICAL GENETICS, 2022, 101 (03) : 307 - 316
  • [46] Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12p
    Sharma, Pankaj
    Gupta, Neerja
    Chowdhury, Madhumita R.
    Sapra, Savita
    Shukla, Rashmi
    Lall, Meena
    Kabra, Madhulika
    JOURNAL OF PEDIATRIC GENETICS, 2013, 2 (03) : 163 - 169
  • [47] 8q Gains and 8p Losses Are Associated To Even Worse Outcome in Patients With Chronic Lymphocytic Leukemia (CLL) and Del(17p)
    Espinet, Blanca
    Blanco, Gonzalo
    Puiggros, Anna Maria
    Rodriguez-Rivera, Maria
    Garcia-Malo, Ma Dolores
    Ortega, Margarita
    Calasanz, Ma Jose
    Luno, Elisa
    Vargas, Ma Teresa
    Grau, Javier
    Martinez-Laperche, Carolina
    Valiente, Alberto
    Lopez-Pavia, Maria
    Pinan, Ma Angeles
    Hernandez-Rivas, Jesus Ma
    Batlle-Lopez, Ana
    Salido, Marta
    Ardanaz, Maite
    Coado, Rosa
    LABORATORY INVESTIGATION, 2015, 95 : 343A - 343A
  • [48] Deletion of 8p: a report of a child with normal intelligence
    Gilmore, L
    Cuskelly, M
    Jobling, A
    Smith, S
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2001, 43 (12): : 843 - 846
  • [49] 8q Gains and 8p Losses Are Associated To Even Worse Outcome in Patients With Chronic Lymphocytic Leukemia (CLL) and Del(17p)
    Espinet, Blanca
    Blanco, Gonzalo
    Maria Puiggros, Anna
    Rodriguez-Rivera, Maria
    Dolores Garcia-Malo, Ma
    Ortega, Margarita
    Jose Calasanz, Ma
    Luno, Elisa
    Teresa Vaigas, Ma
    Grau, Javier
    Martinez-Laperche, Carolina
    Valiente, Alberto
    Lopez-Pavia, Maria
    Angeles Pinan, Ma
    Ma Hernandez-Rivas, Jesus
    Batlle-Lopez, Ana
    Salido, Marta
    Ardanaz, Maite
    Collado, Rosa
    MODERN PATHOLOGY, 2015, 28 : 343A - 343A
  • [50] PARTIAL TRISOMY AND MONOSOMY 8P DUE TO INVERSION DUPLICATION
    ENGELEN, JJM
    DEDIESMULDERS, CEM
    FRYNS, JP
    HOOVERS, JMN
    ALBRECHTS, JCM
    LOOTS, WJG
    JACOBS, ME
    HAMERS, AJH
    CLINICAL GENETICS, 1994, 45 (04) : 203 - 207