A Case of Early Onset Scoliosis with Trisomy 1q and Monosomy 21q

被引:1
|
作者
Fukase, Yuta [1 ]
Watanabe, Kota [1 ]
Takeda, Kazuki [1 ]
Okubo, Toshiki [1 ]
Suzuki, Satoshi [1 ]
Tsuji, Osahiko [1 ]
Nagoshi, Narihito [1 ]
Yagi, Mitsuru [1 ,2 ]
Nakamura, Masaya [1 ]
机构
[1] Keio Univ, Sch Med, Dept Orthoped Surg, Tokyo, Japan
[2] Int Univ Hlth & Welf, Sch Med, Dept Orthoped Surg, Chiba, Japan
来源
SPINE SURGERY AND RELATED RESEARCH | 2024年 / 8卷 / 06期
关键词
Early onset scoliosis; Trisomy; Monosomy; Surgical Site Infection; TITANIUM RIB VEPTR; COMPLICATIONS;
D O I
10.22603/ssrr.2024-0099
中图分类号
R61 [外科手术学];
学科分类号
摘要
引用
收藏
页码:654 / 658
页数:5
相关论文
共 50 条
  • [31] Genomic analysis of partial 21q monosomies with variable phenotypes
    Roberson, Elisha D. O.
    Wohler, Elizabeth Squibb
    Hoover-Fong, Julie E.
    Lisi, Emily
    Stevens, Eric L.
    Thomas, George H.
    Leonard, Jay
    Hamosh, Ada
    Pevsner, Jonathan
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2011, 19 (02) : 235 - 238
  • [32] Complete trisomy 1q with mosaic Y;1 translocation: A recurrent aneuploidy presenting diagnostic dilemmas
    Scheuerle, A
    Heller, K
    Elder, F
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 138A (02) : 166 - 170
  • [33] Genomic analysis of partial 21q monosomies with variable phenotypes
    Elisha D O Roberson
    Elizabeth Squibb Wohler
    Julie E Hoover-Fong
    Emily Lisi
    Eric L Stevens
    George H Thomas
    Jay Leonard
    Ada Hamosh
    Jonathan Pevsner
    European Journal of Human Genetics, 2011, 19 : 235 - 238
  • [34] PRENATAL-DIAGNOSIS OF PARTIAL TRISOMY 1Q USING FLUORESCENT IN-SITU HYBRIDIZATION
    DUPONT, BR
    HUFF, RW
    RIDGWAY, LE
    STRATTON, RF
    MOORE, CM
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 50 (01): : 21 - 27
  • [35] CYTOGENETIC ANALYSIS OF UVEAL MELANOMA - CONSISTENT OCCURRENCE OF MONOSOMY 3 AND TRISOMY 8Q
    HORSMAN, DE
    WHITE, VA
    CANCER, 1993, 71 (03) : 811 - 819
  • [36] Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation
    Tinsa, F.
    Chebbi, Y.
    Meddeb, M.
    Bousnina, D.
    Boussetta, K.
    Bousnina, S.
    JOURNAL OF APPLIED GENETICS, 2009, 50 (03) : 289 - 291
  • [37] Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26)
    Tsukuda, T
    Nagata, I
    Sawada, H
    Murakami, J
    Hanaki, K
    Urashima, H
    Kaneda, T
    Shimizu, N
    Kaibara, M
    Kodama, N
    Ohzeki, T
    Shiraki, K
    CLINICAL GENETICS, 1996, 50 (04) : 220 - 222
  • [38] Clinical features of a case with trisomy 10q and monosomy 3p resulting from a maternal balanced translocation
    Mahjoubi, Frouzandeh
    Akbari, Mohammad Taghi
    Babamohammadi, Gholamreza
    JOURNAL OF PEDIATRIC NEUROLOGY, 2008, 6 (03) : 273 - 276
  • [39] Attenuated phenotype in a child with trisomy for 1q due to unbalanced X:1 translocation [46,X,der(X),t(X;1)(q28;q32.1)]
    Yatsenko, SA
    Sahoo, T
    Rosenkranz, M
    Mendoza-Londono, R
    Naeem, R
    Scaglia, F
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 128A (01) : 72 - 77
  • [40] Chromosome 1q Terminal Deletion and Congenital Glaucoma: A Case Report
    AlSaad, Rakan
    ElMansoury, Jeylan
    AlHazzaa, Selwa A. F.
    Dirar, Qais S.
    AMERICAN JOURNAL OF CASE REPORTS, 2020, 21