A FAMILIAL RECIPROCAL TRANSLOCATION t(1;15) IN THREE GENERATIONS IDENTIFIED IN A REGULAR TRISOMY 21 PATIENT

被引:0
|
作者
Garcia-Delgado, C. [1 ]
Bahena-Martinez, E. [1 ]
Aparicio-Onofre, A. [1 ]
Guevara-Yanez, R.
Cervantes-Peredo, A. [2 ]
Azotla-Vilchis, O. C. [1 ]
Estrada-Mena, J.
Luna-Angulo, A.
Villa-Morales, J. [1 ]
Moran-Barroso, V. F.
机构
[1] Hosp Infantil Mexico Dr Federico Gomez, Dept Genet, Mexico City 06720, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Serv Genet, Fac Med, Mexico City, DF, Mexico
来源
GENETIC COUNSELING | 2010年 / 21卷 / 03期
关键词
Trisomy; 21; Familial translocation; t(1; 15); IN-SITU HYBRIDIZATION; CARRIERS; SPERM; SEGREGATION;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient: The concurrence of a reciprocal translocation and an aneuploidy represent a rare coincidence and an interchromosome effect between these two events has been suggested. We report the case of a family with a t(1;15) in three generations which was identified through the evaluation of a patient with classical trisomy 21 or Down syndrome. The cytogenetic analysis with GTG banding showed that the proband had a regular trisomy 21 and a balanced translocation t(1;15). FISH and microsatellite analysis were carried out in the family in order to discard an interchromosomal effect. The implications for genetic assessment are discussed.
引用
收藏
页码:299 / 306
页数:8
相关论文
共 50 条
  • [1] Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis
    Prontera, Paolo
    Buldrini, Barbara
    Aiello, Vincenzo
    Gruppioni, Rita
    Bonfatti, Alessandra
    Venti, Giovanna
    Ferlini, Alessandra
    Sensi, Alberto
    Calzolari, Elisa
    Donti, Emilio
    PRENATAL DIAGNOSIS, 2006, 26 (06) : 571 - 576
  • [2] A de novo reciprocal t(2;18) translocation with regular trisomy 21
    Cyrus, Cyril
    Kaur, Harpreet
    Koshy, Teena
    Thankanadar, Jegatheesan
    Nallathambi, Chandra
    GENETIC TESTING, 2007, 11 (04): : 459 - 462
  • [3] Prenatal diagnosis of a trisomy 21 fetus with an unusual familial t(15;21) translocation
    Kim, KC
    Jackson, KE
    Pridjian, G
    Mao, R
    Li, MM
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 297 - 297
  • [4] FAMILIAL RECIPROCAL TRANSLOCATION T(1-4)(Q31-P15) TRACED THROUGH 5 GENERATIONS
    MARTINLUCAS, MA
    PEREZCASTILLO, A
    ABRISQUETA, JA
    CYTOGENETICS AND CELL GENETICS, 1985, 39 (03): : 237 - 237
  • [5] Familial reciprocal translocation t(1;5)(q23;p12), three cases in two generations
    Gug, Cristina
    Cioata, Ionel
    Cretu, Anca
    Tuduce, Ioana
    CHROMOSOME RESEARCH, 2007, 15 : 69 - 69
  • [6] FAMILIAL MONGOLISM (TRISOMY-21 SYNDROME) RESULTING FROM A 15/21 CHROMOSOME TRANSLOCATION IN MORE THAN 3 GENERATIONS OF A LARGE KINDRED
    MACINTYRE, MN
    STAPLES, WI
    HEMPEL, JM
    STEINBERG, AG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1962, 14 (04) : 335 - &
  • [7] DOUBLE AUTOSOMAL ABERRATION - TRISOMY-21 AND FAMILIAL RECIPROCAL TRANSLOCATION T(10-12)(P14-Q21)
    BUTOMO, IV
    MASHKOVA, MV
    TSITOLOGIYA, 1977, 19 (11): : 1291 - 1296
  • [8] Familial Robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21
    Mau, UA
    Petruch, UR
    Kaiser, P
    Eggermann, T
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2000, 8 (11) : 815 - 819
  • [9] Familial Robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21
    Ulrike A Mau
    Uwe R Petruch
    Peter Kaiser
    Thomas Eggermann
    European Journal of Human Genetics, 2000, 8 : 815 - 819
  • [10] DISTAL 15Q TRISOMY AND FAMILIAL T(15,21)(Q24,Q22) TRANSLOCATION
    VIANELLO, MG
    FASCE, L
    VENZANO, V
    BESIO, B
    IESTER, A
    CORDONE, G
    RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS, 1986, 12 (02): : 166 - 170