MULTIPLE ABNORMALITIES IN A CHILD WITH PARTIAL DUPLICATIONS OF 10P AND 13Q FROM A 3-1 SEGREGATION OF A MATERNAL T(10-13) TRANSLOCATION

被引:4
|
作者
YIP, MY
WILLIAMS, J
GODDARD, A
CAMPBELL, P
LAMBERT, I
SMITHELLS, RW
机构
[1] ST JAMES UNIV HOSP,REG CYTOGENET UNIT,LEEDS LS9 7TF,W YORKSHIRE,ENGLAND
[2] PRINCE WALES HOSP,DEPT MED GENET,SYDNEY,NSW,AUSTRALIA
[3] ROYAL HOSP WOMEN,NEONATAL UNIT,SYDNEY,AUSTRALIA
关键词
D O I
10.1136/jmg.27.3.188
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Partial duplications of 10p and 13q in association with partial deletions of other chromosome segments have been variously reported. We describe here a female child with multiple congenital abnormalities and combined partial duplications of 10p and 13q resulting from a 3:1 segregation of a maternal t(10;13(p13;q22). In comparing the phenotypic features of the two chromosome imbalances, the expression of features typical of partial duplication 10p appeared more pronounced.
引用
收藏
页码:188 / 191
页数:4
相关论文
共 50 条
  • [41] PARTIAL 13 TRISOMY IN A NEONATE BY MATERNAL 46, XX, T (3,13) (P26, Q21)
    STOLL, C
    HALB, A
    PEDIATRIE, 1974, 29 (07): : 725 - 729
  • [42] Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers
    Escudero, T
    Lee, M
    Carrel, D
    Blanco, J
    Munné, S
    PRENATAL DIAGNOSIS, 2000, 20 (07) : 599 - 602
  • [43] PARTIAL TRISOMY-6P AND PARTIAL TRISOMY-22 RESULTING FROM 3-1 MEIOTIC DISJUNCTION OF MATERNAL (6P-22Q) TRANSLOCATION
    SCARBROUGH, PR
    CARROLL, AJ
    FINLEY, SC
    HAMERICK, K
    JOURNAL OF MEDICAL GENETICS, 1986, 23 (02) : 185 - 187
  • [44] Molecular and cytogenetic characterisation of an unusual case of partial trisomy partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14)
    Gentile, M
    Buonadonna, AL
    Cariola, F
    Fiorente, P
    Valenzano, MC
    Guanti, G
    JOURNAL OF MEDICAL GENETICS, 1999, 36 (01) : 77 - 82
  • [45] Isochromosome (17)(q10) and translocation (4;12)(q12;p13) in a child with acute myeloid leukemia
    Nathan, PC
    Chun, K
    Abdelhaleem, M
    Malkin, D
    CANCER GENETICS AND CYTOGENETICS, 2001, 131 (01) : 82 - 85
  • [46] 10p15.3p13 duplication inherited from paternal balance translocation (46,XY,t(5;10)(q35.1;p13)) identified on non-invasive prenatal testing
    Mei, Jin
    Wang, Hao
    Zhan, Liyong
    JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, 2017, 43 (06) : 1076 - 1079
  • [47] Abnormalities of chromosome 1p/q are highly associated with chromosome 13/13q deletions and are an adverse prognostic factor for the outcome of high-dose chemotherapy in patients with multiple myeloma
    Wu, Ka Lung
    Beverloo, Berna
    Lokhorst, Henk M.
    Segeren, Christine M.
    van der Holt, Bronno
    Steijaert, Monique M.
    Westveer, Petra H.
    Poddighe, Pino J.
    Verhoef, Gregor E.
    Sonneveld, Pieter
    BRITISH JOURNAL OF HAEMATOLOGY, 2007, 136 (04) : 615 - 623
  • [48] A Case of Partial Trisomy of 10q and Partial Monosomy of 6p Resulting from Maternal t(6;10) (p23;q24)
    Sabnis, Anjali Satyen
    Pais, Anurita S.
    Pradhan, Gauri
    JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2021, 15 (08) : GD1 - GD3
  • [49] Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney
    O'Meara, Elaine
    Stack, Deirdre
    Lee, Cheng-Han
    Garvin, A. Julian
    Morris, Thomas
    Argani, Pedram
    Han, Jeong S.
    Karlsson, Jenny
    Gisselson, David
    Leuschner, Ivo
    Gessler, Manfred
    Graf, Norbert
    Fletcher, Jonathan A.
    O'Sullivan, Maureen J.
    JOURNAL OF PATHOLOGY, 2012, 227 (01): : 72 - 80
  • [50] A new translocation partner for CBFB in acute myeloid leukemia, t(10;16)(p13;q22)
    Steinberg, Jordan
    Karp, Lynne
    Mahmood, Nayyara
    Jodlowski, Eric
    Patel, Palak
    Salyanna, Muhammad
    Doddapaneni, Padma
    Roda, Maricris
    Revelosanchez, Ana
    Gheewala, Dipti
    Gur, Deniz
    Shaham, Meira
    Cohen, Ninette
    MOLECULAR GENETICS AND METABOLISM, 2021, 132 : S40 - S40