2 ADDITIONAL CASES OF ISOCHROMOSOME 21Q OR TRANSLOCATION 21Q21Q IN HEMATOLOGICAL MALIGNANCIES

被引:10
作者
HURET, JL
SCHOENWALD, M
GABARRE, J
VAUGIER, GL
TANZER, J
机构
[1] CNRS,URA 1338,F-86022 POITIERS,FRANCE
[2] HOP LA PITIE SALPETRIERE,PARIS,FRANCE
关键词
ISOCHROMOSOME; 21Q; LEUKEMIAS; TRANSLOCATION; 21Q21Q;
D O I
10.1159/000204815
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report on 2 patients with isochromosome 21q [i(21q)] or translocation 21q21q [t(21q21q)] in myeloid disorders. Of 18 available cases of i(21q) or t(21q21q), 15 were found in myeloid malignancies, often secondary to a previous carcinogen exposure. Complex karyotypes were found in most cases. Four cases presented with i(21q) or t(21q21q) as the sole anomaly, and this might represent a specific entity.
引用
收藏
页码:111 / 114
页数:4
相关论文
共 50 条
  • [1] Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21
    Riegel, M
    Hargreaves, P
    Baumer, A
    Guc-Scekic, M
    Ignjatovic, M
    Schinzel, A
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2005, 48 (02) : 167 - 174
  • [2] MOLECULAR ANALYSIS TO ASSIGN PARENTAL ORIGIN AND DISTINGUISH DE-NOVO I(21Q) FROM T(21Q21Q) IN 2 DOWN-SYNDROME FETUSES
    ZHAO, J
    THARAPEL, AT
    SHULMAN, LP
    SIMPSON, JL
    ELIAS, S
    JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 1994, 1 (02) : 128 - 130
  • [3] Acute myelogenous leukaemia with t(8;21) translocation of normal cell origin in mosaic Down's syndrome with isochromosome 21q
    Sato, A
    Imaizumi, M
    Koizumi, Y
    Obara, Y
    Nakai, H
    Noro, T
    Saito, T
    Saisho, T
    Yoshinari, M
    Cui, Y
    Suzuki, H
    Funato, T
    Iinuma, K
    BRITISH JOURNAL OF HAEMATOLOGY, 1997, 96 (03) : 614 - 616
  • [4] FURTHER CHARACTERIZATION OF 19 CASES OF REA(21Q21Q) AND DELINEATION AS ISOCHROMOSOMES OR ROBERTSONIAN TRANSLOCATIONS IN DOWN-SYNDROME
    SHAFFER, LG
    MCCASKILL, C
    HALLER, V
    BROWN, JA
    JACKSONCOOK, CK
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (08): : 1218 - 1222
  • [5] Subtelomeric trisomy 21q: A new benign chromosomal variant
    Bonaglia, Maria Clara
    Marelli, Susan
    Gottardi, Giulietta
    Zucca, Claudio
    Pramparo, Tiziano
    Giorda, Roberto
    Grasso, Rita
    Borgatti, Renato
    Zuffardi, Orsetta
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2007, 50 (01) : 54 - 59
  • [6] Paternal meiotic origin of der(21;21)(q10;q10) mosaicism [46,XX/46,XX,der(21;21)(q10;q10),+21] in a girl with mild Down syndrome
    Dieter Kotzot
    Albert Schinzel
    European Journal of Human Genetics, 2000, 8 : 709 - 712
  • [7] Paternal meiotic origin of der(21;21)(q10;q10) mosaicism [46,XX/46,XX,der(21;21)(q10;q10),+21] in a girl with mild Down syndrome
    Kotzot, D
    Schinzel, A
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2000, 8 (09) : 709 - 712
  • [8] TRANSLOCATION (3-21)(Q26-Q22) IN SECONDARY LEUKEMIA - REPORT OF 2 CASES AND LITERATURE-REVIEW
    SCHNEIDER, NR
    BOWMAN, WP
    FRENKEL, EP
    ANNALES DE GENETIQUE, 1991, 34 (3-4): : 256 - 263
  • [9] Detection of paternal origin of fetal de novo rea(21q;21q) down syndrome in a pregnancy of a young woman associated with an abnormal first-trimester maternal serum screening result
    Chen, Chih-Ping
    Jou, Quan-Bin
    Chern, Schu-Rern
    Chen, Shin-Wen
    Wu, Fang-Tzu
    Chen, Wen-Lin
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2022, 61 (02): : 356 - 358
  • [10] A case with Down syndrome presenting 21q22q translocation:: Differential diagnosis
    Guenes, Sezgin
    Kara, Nurten
    Guenal, Nazlihan
    Kuecuekoeduek, Suekrue
    Oekten, Guelsen
    Tural, Senguel
    Taskin, Emre
    TURKIYE KLINIKLERI TIP BILIMLERI DERGISI, 2007, 27 (06): : 928 - 929