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
  • [31] MATERNAL SERUM SCHWANGERSCHAFTS PROTEIN-1 (SP1) AND FETAL CHROMOSOMAL-ABNORMALITIES AT 10-13 WEEKS GESTATION
    BRIZOT, ML
    BERSINGER, NA
    XYDIAS, G
    SNIJDERS, RJM
    NICOLAIDES, KH
    EARLY HUMAN DEVELOPMENT, 1995, 43 (01) : 31 - 36
  • [32] Familial translocation t(3;10)(p26;p12) leading to partial trisomy 10p(12 > pter): segregation, molecular cytogenetics analysis and clinical phenotype in four generation
    Nucaro, A. L.
    Melis, P.
    Meloni, M.
    Corona, S.
    Rossino, R.
    Loi, M.
    Boccone, L.
    Cianchetti, C.
    CHROMOSOME RESEARCH, 2005, 13 : 72 - 72
  • [33] A novel translocation t(8;10)(q12;p13) in acute myeloid leukemia
    Talavera Yaguez, M.
    Ferro, M. T.
    Villalon, C.
    de Leon, A.
    Garcia-Sagredo, J. A.
    Garcia Miguel, P.
    Polo, M.
    San Roman, C.
    CHROMOSOME RESEARCH, 2007, 15 : 204 - 205
  • [34] Segregation pedigree analysis of t(2,13)(p25.1,q33.1) carriers and description of the resulting partial trisomy 2p and monosomy 13q phenotype in progeny
    Panasiuk, B.
    Midro, A. T.
    Wierzba, J.
    Lipska-Zietkiewicz, B. S.
    Stasiewicz-Jarocka, B.
    Koczkowska, M.
    Limon, J.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 499 - 499
  • [35] Male factor infertility associated with a familial translocation t(1;13)(q24;q10)
    Sazci, A
    Ercelen, N
    Ergul, E
    Akpinar, G
    FERTILITY AND STERILITY, 2005, 83 (05) : 1548 - 1548
  • [36] Phenotype-cytogenetic correlation in partial trisomy 13q and trisomy 18p resulting from maternal origin
    Eid, Maha M.
    Eid, Ola M.
    Mohamed, Amal M.
    Abdelghany, Asia E.
    Kader, Rania M. A. Abdel
    Taher, Mohamed B.
    Sayed-Ahmed, Mohammed M.
    Salam, Ghada M. H. Abdel
    Afifi, Hanan H.
    HUMAN GENE, 2025, 43
  • [37] PARTIAL-8 TRISOMY BY 3 - 1 SEGREGATION OF BALANCED MATERNAL TRANSLOCATION T(6Q+-8Q-)
    KOGAME, K
    KUDO, H
    JAPANESE JOURNAL OF HUMAN GENETICS, 1985, 30 (03): : 239 - 248
  • [38] PROXIMAL 15Q TRISOMY FROM IMPROPER SEGREGATION OF MATERNAL TRANSLOCATION T(10 - 15(Q26Q15)
    VARGAS, AJ
    MAULINO, N
    ARCHIVOS DE BIOLOGIA Y MEDICINA EXPERIMENTALES, 1981, 14 (01): : 89 - 89
  • [39] A biphenotypic T and B acute leukemia with t(10;11)(p13;q21) translocation.
    Pereira, J
    Tutiya, IEK
    Beitler, B
    Martinez, GA
    Velloso, EERP
    Pinheiro, ED
    Kumeda, CA
    Conchon, M
    Chamone, D
    BLOOD, 2001, 98 (11) : 206B - 206B
  • [40] Partial duplication of 3Q and distal deletion of 10Q inherited from a maternal balanced translocation
    Su, PH
    Chen, JY
    Chen, SJ
    Hung, HM
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2004, 103 (11) : 853 - 857