Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1-q26.3

被引：12
|
作者：
Carter, Melissa T. [1 ]
Dyack, Sarah [3 ]
Richer, Julie [2 ]
机构：
[1] Bloorview Kids Rehab, Div Dev Paediat, Toronto, ON M4G 1R8, Canada
[2] Childrens Hosp Eastern Ontario, Eastern Ontario Reg Genet Program, Ottawa, ON K1H 8L1, Canada
[3] Dalhousie Univ, IWK Hlth Ctr, Halifax, NS, Canada
来源：
CLINICAL DYSMORPHOLOGY | 2010年 / 19卷 / 03期
关键词：
D O I：
10.1097/MCD.0b013e3283377915
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
[No abstract available]
引用
收藏
页码：140 / 145
页数：6
相关论文
共 50 条
  • [31] Two cases of distal trisomy 10q resulting from maternal balanced translocation
    Akbas, H.
    Oral, D.
    Yildirim, R.
    Fidanboy, M.
    Budak, T.
    CHROMOSOME RESEARCH, 2007, 15 : 129 - 130
  • [32] Partial trisomy of 15pter-q15 and 10q24-qter segments in a newborn compared to the duplication 10q syndrome.
    Gowans, G
    Berry, T
    Christensen, K
    Hersh, J
    Yen, F
    GENETICS IN MEDICINE, 2004, 6 (04) : 320 - 320
  • [33] Distal Monosomy 10q Presented as Congenital Hypothyroidism
    Braha, Elena Emanuela
    Rusu, Cristina
    Armasu, Ioana
    Belceanu, Alina
    Popescu, Roxana
    Bursuc, Anamaria
    Vulpoi, Carmen
    HORMONE RESEARCH IN PAEDIATRICS, 2016, 86 : 504 - 504
  • [34] BALANCED TRANSLOCATION (10-13) IN A FATHER, ASCERTAINED THROUGH THE STUDY OF MEIOSIS IN SEMEN, AND PARTIAL TRISOMY 10Q IN HIS SON - CHARACTERIZATION OF THE REGION RESPONSIBLE FOR THE PARTIAL TRISOMY 10Q SYNDROME
    MIRO, R
    TEMPLADO, C
    PONSA, M
    SERRADELL, J
    MARINA, S
    EGOZCUE, J
    HUMAN GENETICS, 1980, 53 (02) : 179 - 182
  • [35] Fine mapping of chromosome 10q deletions in mycosis fungoides and Sezary syndrome: Identification of two discrete regions of deletion at 10q23.33-24.1 and 10q24.33-25.1
    Wain, EM
    Mitchell, TJ
    Russell-Jones, R
    Whittaker, SJ
    GENES CHROMOSOMES & CANCER, 2005, 42 (02): : 184 - 192
  • [36] Three's a crowd: 10q triplication secondary to a paternal 10q duplication
    Gardham, Alice
    Sullivan, Caroline
    Bernhard, Birgitta
    CLINICAL DYSMORPHOLOGY, 2014, 23 (04) : 143 - 146
  • [37] DISTAL TRISOMY 10q DUE TO MATERNAL INSERTIONAL TRANSLOCATION (15;10): A CASE REPORT AND REVIEW OF LITERATURE
    Turedi, O.
    Vicdan, A.
    Kutlay, N. Yurur
    GENETIC COUNSELING, 2016, 27 (02): : 273 - 278
  • [38] FAMILIAL PARTIAL TRISOMY 10Q (Q23 -] QTER) SYNDROME AND PARACENTRIC INVERSION 3(Q13Q26) IN SAME PATIENT
    BASS, HN
    SPARKES, RS
    CRANDALL, BF
    TANNENBAUM, SM
    ANNALES DE GENETIQUE, 1978, 21 (02): : 74 - 77
  • [39] PARTIAL TRISOMY 10Q (10Q25.1→QTER) AN PARTIAL MONOSOMY 13Q (13Q34→QTER) PRESENTING WITH FETAL PYELECTASIS: PRENATAL DIAGNOSIS AND ARRAY COMPARATIVE GENOMIC HYBRIDIZATION CHARACTERIZATION
    Chen, Chih-Ping
    Su, Yi-Ning
    Tsai, Fuu-Jen
    Chern, Schu-Rern
    Hsu, Chin-Yuan
    Wu, Pei-Chen
    Lee, Chen-Chi
    Chen, Wen-Lin
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2010, 49 (04): : 539 - 543
  • [40] A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11->q2237
    VanBuggenhout, G
    Decock, P
    Fryns, JP
    GENETIC COUNSELING, 1996, 7 (01): : 53 - 59
12345