Cryptic deletion of EGR1 in association with a novel balanced t(5;22)(q31;q11.2) in a patient with myelodysplastic syndrome

被引:3
|
作者
Hoffman, Matthew W.
Janney, Stephen [4 ]
Batanian, Jacqueline R. [1 ,2 ,3 ]
机构
[1] St Louis Univ, Sch Med, Dept Pediat, St Louis, MO 63104 USA
[2] St Louis Univ, Sch Med, Dept Pathol, St Louis, MO 63104 USA
[3] SSM Cardinal Glennon Childrens Med Ctr, Mol Cytogenet Lab, St Louis, MO 63104 USA
[4] St Marys Hlth Ctr, St Louis, MO 63117 USA
关键词
CHROMOSOME; GENE; 5Q;
D O I
10.1016/j.cancergencyto.2009.02.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Loss of chromosome 5 or deletion of 5q is commonly seen in patients with myelodysplastic syndrome (MDS). Loss of EGR1, located on 5q31, has been postulated as contributing to the pathology of MDS in patients with -5/del(5q). We report on the first case of a patient with a novel apparent balanced translocation between chromosomes 5 and 22 at breakpoints 5q31 and 22q11.2. Fluorescence in situ hybridization using a probe of EGR1 detected a cryptic deletion masked by the translocation. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:106 / 108
页数:3
相关论文
共 50 条
  • [31] MYELODYSPLASTIC SYNDROME IN A PATIENT WITH A UNIQUE CONSTITUTIONAL CHROMOSOME ABNORMALITY T(2,11) (Q31,P13)
    HINODA, Y
    ITOH, H
    TAKAHASHI, T
    ADACHI, M
    TSUJISAKI, M
    IMAI, K
    YACHI, A
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 1992, 56 (01) : 95 - 97
  • [32] Translocation (1;22)(p36;q11.2) with concurrent del(22)(q11.2) resulted in homozygous deletion of SNF5/INI1 in a newly established cell line derived from extrarenal rhabdoid tumor
    Akiko Misawa
    Hajime Hosoi
    Issei Imoto
    Tomoko Iehara
    Tohru Sugimoto
    Johji Inazawa
    Journal of Human Genetics, 2004, 49 : 586 - 589
  • [33] Association of a functional Claudin-5 variant with schizophrenia in female patients with the 22q11.2 deletion syndrome
    Guo, Yiran
    Singh, Larry N.
    Zhu, Yuankun
    Gur, Raquel E.
    Resnick, Adam
    Anderson, Stewart A.
    Alvarez, Jorge I.
    SCHIZOPHRENIA RESEARCH, 2020, 215 : 451 - 452
  • [34] A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome
    Prescott, K
    Woodfine, K
    Stubbs, P
    Super, M
    Kerr, B
    Palmer, R
    Carter, NP
    Scambler, P
    HUMAN GENETICS, 2005, 116 (1-2) : 83 - 90
  • [35] A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome
    Prescott, K
    Woodfine, K
    Stubbs, P
    Super, M
    Kerr, B
    Palmer, R
    Carter, NP
    Scambler, P
    JOURNAL OF MEDICAL GENETICS, 2004, 41 : S68 - S68
  • [36] Myelodysplastic syndrome with t(9;22)(p24;q11.2), a BCR-JAK2 fusion: case report and review of the literature
    Kantarcioglu, Bulent
    Kaygusuz-Atagunduz, Isik
    Uzay, Ant
    Toptas, Tayfur
    Tuglular, Tulin Firatli
    Bayik, Mahmut
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2015, 102 (03) : 383 - 387
  • [37] A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome
    Katrina Prescott
    Kathryn Woodfine
    Paula Stubbs
    Maurice Super
    Bronwyn Kerr
    Rodger Palmer
    Nigel P. Carter
    Peter Scambler
    Human Genetics, 2005, 116 : 83 - 90
  • [38] Myelodysplastic syndrome with t(9;22)(p24;q11.2), a BCR-JAK2 fusion: case report and review of the literature
    Bulent Kantarcioglu
    Isik Kaygusuz-Atagunduz
    Ant Uzay
    Tayfur Toptas
    Tulin Firatli Tuglular
    Mahmut Bayik
    International Journal of Hematology, 2015, 102 : 383 - 387
  • [39] Myelodysplastic syndrome with t(5;12)(q31;p12-p13) and eosinophilia: A pediatric case with review of literature
    Pellier, I
    LeMoine, PJ
    Rialland, X
    Francois, S
    Baranger, L
    Blanchet, O
    LargetPiet, L
    Ifrah, N
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1996, 18 (03) : 285 - 288
  • [40] Aplastic anemia evolving into overt myelodysplastic syndrome/acute myeloid leukemia with t(3;5)(p25;q31)
    Kawata, E
    Kuroda, J
    Kimura, S
    Kamitsuji, Y
    Kobayashi, Y
    Yoshikawa, T
    CANCER GENETICS AND CYTOGENETICS, 2002, 137 (02) : 91 - 94