DE-NOVO TANDEM DUPLICATION OF CHROMOSOME SEGMENT 22QLL-Q12 - CLINICAL, CYTOGENETIC, AND MOLECULAR CHARACTERIZATION

被引:29
作者
LINDSAY, EA
SHAFFER, LG
CARROZZO, R
GREENBERG, F
BALDINI, A
机构
[1] BAYLOR COLL MED,DEPT MOLEC & HUMAN GENET,HOUSTON,TX 77030
[2] BAYLOR COLL MED,CTR HUMAN GENOME,HOUSTON,TX 77030
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 56卷 / 03期
关键词
CHROMOSOME; 22; DUPLICATION; CAT-EYE SYNDROME; CONGENITAL HEART DEFECT;
D O I
10.1002/ajmg.1320560316
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a case of duplication of the segment 22q11-q12 due to a de novo duplication. Molecular cytogenetics studies demonstrated this to be a tandem duplication, flanked proximally by the marker D22Z4, a centromeric alpha satellite DNA repeat, and distally by D22S260, an anonymous DNA marker proximal to the Ewing sarcoma breakpoint. The segment includes the regions responsible for the ''cat-eye,'' Di George, and velo-cardio-facial syndromes and extends distal to the breakpoint cluster region (BCR). The clinical picture is dominated by the cardiac defects and includes findings reminiscent of ''cat-eye'' syndrome. These findings reinforce the hypothesis that the proximal 22q region contains dosage-sensitive genes involved in development. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:296 / 299
页数:4
相关论文
共 42 条
  • [1] A DE-NOVO 6Q11-Q15 DUPLICATION INVESTIGATED BY CHROMOSOME PAINTING
    GIARDINO, D
    RIZZI, N
    BRISCIOLI, V
    BETTIO, D
    CLINICAL GENETICS, 1994, 46 (05) : 377 - 379
  • [2] CHARGE ASSOCIATION IN A CHILD WITH DE-NOVO INVERTED DUPLICATION (14)(Q22-]Q24.3)
    NORTH, KN
    WU, BL
    CAO, BN
    WHITEMAN, DAH
    KORF, BR
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 57 (04): : 610 - 614
  • [3] DE-NOVO PROXIMAL INTERSTITIAL DELETIONS OF 14Q - CYTOGENETIC AND MOLECULAR INVESTIGATIONS
    SHAPIRA, SK
    ANDERSON, KL
    ORRURTREGAR, A
    CRAIGEN, WJ
    LUPSKI, JR
    SHAFFER, LG
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 52 (01): : 44 - 50
  • [4] De novo direct tandem duplication of a small segment of the short arm of chromosome 7 (p21.22->22.1)
    Franz, HBG
    Schliephacke, M
    Niemann, G
    Mielke, G
    Backsch, C
    CLINICAL GENETICS, 1996, 50 (05) : 426 - 429
  • [5] Prenatal detection and molecular characterization of a de novo duplication of the distal long arm of chromosome 19
    Cotter, PD
    McCurdy, LD
    Gershin, IF
    Babu, A
    Willner, JP
    Desnick, RJ
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 71 (03): : 325 - 328
  • [6] Molecular cytogenetic characterization and origin of two de novo duplication 9p cases
    Tsezou, A
    Kitsiou, S
    Galla, A
    Petersen, MB
    Karadima, G
    Syrrou, M
    Sahlèn, S
    Blennow, E
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 91 (02): : 102 - 106
  • [7] A De Novo 22q11.22q11.23 Interchromosomal Tandem Duplication in a Boy With Developmental Delay, Hyperactivity, and Epilepsy
    Shimojima, Keiko
    Imai, Katsumi
    Yamamoto, Toshiyuki
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (11) : 2820 - 2826
  • [8] Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement
    Zhou, Yang
    Yao, Qi
    Cui, Ying-Xia
    Yao, Bing
    Fan, Kai
    Xia, Xin-Yi
    Hu, Yu-An
    Li, Xiao-Jun
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161A (04) : 897 - 900
  • [9] Molecular cytogenetic and phenotypic characterization of Phelan McDermid and 22q13 duplication syndrome: a case report
    Khalifa, Yousif
    Hassan, Hisham Y. Y.
    Weise, Anja
    Liehr, Thomas
    Alkhayyat, Haya
    MOLECULAR CYTOGENETICS, 2022, 15 (01)
  • [10] Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin
    Chen, Chih-Ping
    Wang, Liang-Kai
    Chern, Schu-Rern
    Wu, Peih-Shan
    Chen, Shin-Wen
    Wu, Fang-Tzu
    Chen, Yun-Yi
    Chen, Wen-Lin
    Chen, Li-Feng
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2020, 59 (05): : 766 - 769