Jumping translocation of 15q24-qter resulting in partial trisomy: A case report

被引:3
|
作者
Czako, Marta [1 ]
Hadzsiev, Kinga [1 ]
Melegh, Bela [1 ]
Kosztolanyi, Gyoergy [1 ]
机构
[1] Univ Pecs, Dept Med Genet, H-7623 Pecs, Hungary
关键词
Hemihypertrophy; Instability; Non-reciprocal translocation; Interstitial telomeric sequence; Mosaicism; Chromosome; 15; INTERSTITIAL TELOMERIC SEQUENCES; 15Q;
D O I
10.1016/j.gene.2012.04.022
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a jumping translocation with five different cell lines detected in four tissues in a 2-year-old patient. This rare type of chromosomal abnormality (not more than 30 cases published so far) proved to be a series of non-reciprocal translocations of the 15q24-qter donor chromosome segment to the telomeric region of chromosomes 5q, 10q, 16q and 19p, respectively. The process, in addition to a few cells without translocation, resulted in partial trisomy of 15q24-qter which was associated with somatic overdevelopment in the patient, with hemihypertrophy and minor anomalies. The phenotype of our patient was different from that of the other two patients found in the literature having the same donor chromosome segment involved in a similar rearrangement. Possibly, the difference in the phenotype lies in the various ratios of somatic mosaicism with five cell lines, in particular the presence of normal one which is extremely rare in patients with jumping translocation. Here we discuss the various ways on how the rearrangement could arise. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:155 / 159
页数:5
相关论文
共 50 条
  • [1] Monosomy and trisomy of 15q24-qter with cleft lip and palate
    Abe, A.
    Hatano, Y.
    Kurita, K.
    Nakano, M.
    Shimizu, M.
    Yokoi, T.
    Sugiyama, N.
    INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2008, 37 (05) : 487 - 490
  • [2] A Case of Partial Trisomy 15q25.3-qter
    Kim, Ji-Hae
    Lee, Won-Mok
    Ryoo, Nam-Hee
    Ha, Jung-Sook
    Jeon, Dong-Seok
    Kim, Jae-Ryong
    Kim, Joon-Sik
    Lee, So-Young
    KOREAN JOURNAL OF LABORATORY MEDICINE, 2009, 29 (01): : 66 - 70
  • [3] PARTIAL TRISOMY 14Q24-]QTER
    ROMAIN, DR
    COLUMBANOGREEN, LM
    SMYTHE, RH
    PARFITT, RG
    GEBBIE, O
    CHAPMAN, CJ
    WALL, M
    JOURNAL OF MEDICAL GENETICS, 1983, 20 (06) : 466 - 467
  • [4] MONOSOMY AND TRISOMY OF 15Q24-]QTER IN A FAMILY WITH A TRANSLOCATION T(6-15)(P25-Q24)
    KRISTOFFERSSON, U
    HEIM, S
    MANDAHL, N
    SUNDKVIST, L
    SZELEST, J
    HAGERSTRAND, I
    CLINICAL GENETICS, 1987, 32 (03) : 169 - 171
  • [5] COMPLEX CHROMOSOME REARRANGEMENT RESULTING IN TRISOMY-15Q22-QTER
    SCARBROUGH, PR
    HOWARDPEEBLES, PN
    FINLEY, WH
    FINLEY, SC
    AMERICAN JOURNAL OF HUMAN GENETICS, 1981, 33 (06) : A119 - A119
  • [6] A COMPLEX CHROMOSOME REARRANGEMENT RESULTING IN TRISOMY 15Q22-]QTER
    HOWARDPEEBLES, PN
    SCARBROUGH, PR
    SHARPE, J
    FINLEY, WH
    FINLEY, SC
    JOURNAL OF MEDICAL GENETICS, 1982, 19 (03) : 224 - 227
  • [7] PARTIAL TRISOMY 15(Q25QTER) IN 2 BROTHERS
    KRISTOFFERSSON, U
    BERGWALL, B
    HEREDITAS, 1984, 100 (01) : 7 - 10
  • [8] Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter
    Sarri, C
    Gyftodimou, J
    Avramopoulos, D
    Grigoriadou, M
    Pedersen, W
    Pandelia, E
    Pangalos, C
    Abazis, D
    Kitsos, G
    Vassilopoulos, D
    BrondumNielsen, K
    Petersen, MB
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 70 (01): : 87 - 94
  • [9] A NEW CASE OF PARTIAL TRISOMY-19Q (Q13.2-]QTER) OWING TO AN UNUSUAL MATERNAL TRANSLOCATION
    VALERIO, D
    LAVORGNA, F
    SCALONA, M
    CONTE, A
    JOURNAL OF MEDICAL GENETICS, 1993, 30 (08) : 697 - 699
  • [10] A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature
    Paththinige, C. S.
    Sirisena, N. D.
    Kariyawasam, U. G. I. U.
    Ediriweera, R. C.
    Kruszka, P.
    Muenke, M.
    Dissanayake, V. H. W.
    BMC MEDICAL GENOMICS, 2018, 11