Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: Prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3

被引:14
作者
Chen, Chih-Ping [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Lin, Yi-Hui [8 ]
Chou, Szu-Yuan [8 ,9 ]
Su, Yi-Ning [10 ]
Chem, Schu-Rern [3 ]
Chen, Yu-Ting [3 ]
Town, Dai-Dyi [1 ]
Chen, Wen-Lin [1 ]
Wang, Wayseen [3 ,11 ]
机构
[1] Mackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[2] Mackay Med Coll, Dept Med, New Taipei City, Taiwan
[3] Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan
[4] Asia Univ, Dept Biotechnol, Taichung, Taiwan
[5] China Med Univ, Sch Chinese Med, Coll Chinese Med, Taichung, Taiwan
[6] Natl Yang Ming Univ, Inst Clin & Community Hlth Nursing, Taipei 112, Taiwan
[7] Natl Yang Ming Univ, Dept Obstet & Gynecol, Sch Med, Taipei 112, Taiwan
[8] Taipei Med Univ, Wan Fang Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[9] Natl Yang Ming Univ, Inst Biomed Engn, Taipei 112, Taiwan
[10] Natl Taiwan Univ Hosp, Dept Med Genet, Taipei, Taiwan
[11] Tatung Univ, Dept Bioengn, Taipei 104, Taiwan
来源
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | 2012年 / 51卷 / 01期
关键词
21q interstitial deletion; 21q terminal deletion; mosaicism; prenatal diagnosis; ring chromosome 21; IDENTIFICATION; DUPLICATION; MOTHER; INFANT; TRANSMISSION; MECHANISMS; CANDIDATE; BIPOLAR; REGION; GENES;
D O I
10.1016/j.tjog.2012.01.014
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To present the perinatal findings and molecular cytogenetic characterization of prenatally detected mosaic r(21). Materials, Methods, and Results: A 29-year-old primigravid woman underwent amniocentesis at 22 weeks' gestation because of hyperechogenic cardiac foci and intrauterine growth restriction. Amniocentesis revealed a karyotype of 46,XY,r(21)[15]/45,XY,-21[5]. The parental karyotypes were normal. The woman requested repeat amniocentesis. Oligonucleotide-based array comparative genomic hybridization was applied to the uncultured amniocytes, rapidly detecting a 2.09-Mb deletion of 21q21.1-q21.2 (21,495,262-23,580,815 bp) and a 5.03-Mb deletion of 21q22.3-q22.3 (41,887,412-46,914,715 bp). Cytogenetic analysis revealed a karyotype of 46,XY,r(21)[8]/45,XY,-21[3]/46,XY,idic r(21)[1]. The pregnancy was terminated, and a malformed fetus was delivered with clinodactyly, short big toes, separation between the first and second toes, prominent nasal bridge, downward slanting palpebral fissures, protuberant occiput, prominent forehead, broad anteverted nasal tip, long philtrum, thin upper lip, small mouth, and micrognathia. The placenta had a karyotype of 46,XY,r(21)[83]/45,XY,-21[11]/46,XY,idic r(21)[6], and the cord blood lymphocytes had a karyotype of 46,XY,r(21)[88]/45,XY,-21[9]/46,XY,idic r(21)[3]. Polymorphic DNA marker analysis determined a maternal origin for the deletion. Conclusion: An extra interstitial 21q deletion can be associated with mosaic r(21) in addition to a terminal 21q deletion. aCGH is useful in determining the breakpoints and associated subtle structural abnormalities in cases of prenatally detected ring chromosome in order to facilitate genetic counseling. Copyright (c) 2012, Taiwan Association of Obstetrics & Gynecology. Published by Elsevier Taiwan LLC. All rights reserved.
引用
收藏
页码:71 / 76
页数:6
相关论文
共 39 条
[1]  
ARONSON DC, 1987, CLIN GENET, V31, P48
[2]   Holoprosencephally: An Update on Cytogenetic Abnormalities [J].
Bendavid, Claude ;
Dupe, Valerie ;
Rochard, Lucie ;
Gicquel, Isabelle ;
Dubourg, Christele ;
David, Veronique .
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2010, 154C (01) :86-92
[3]   Ring chromosome 21 and reproductive pattern: a familial case and review of the literature [J].
Bertini, Veronica ;
Valetto, Angelo ;
Uccelli, Angela ;
Tarantino, Enrico ;
Simi, Paolo .
FERTILITY AND STERILITY, 2008, 90 (05) :2004.e1-2004.e5
[4]   MOSAIC RING CHROMOSOME 18, RING CHROMOSOME 18 DUPLICATION/DELETION AND DISOMY 18: PERINATAL FINDINGS AND MOLECULAR CYTOGENETIC CHARACTERIZATION BY FLUORESCENCE IN SITU HYBRIDIZATION AND ARRAY COMPARATIVE GENOMIC HYBRIDIZATION [J].
Chen, Chih-Ping ;
Kuo, Yung-Ting ;
Lin, Shuan Pei ;
Su, Yi Ning ;
Chen, Yann Jang ;
Hsueh, Rui Yuan ;
Lin, Yi Hui ;
Wu, Pei Chen ;
Lee, Chen Chi ;
Chen, Yu Ting ;
Wang, Wayseen .
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2010, 49 (03) :327-332
[5]   Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter) [J].
Chen, CP ;
Chern, SR ;
Lin, CC ;
Wang, TH ;
Li, YC ;
Hsieh, LJ ;
Lee, CC ;
Hua, HM ;
Wang, WS .
PRENATAL DIAGNOSIS, 2006, 26 (04) :313-320
[6]  
Chen CP, 2004, GENET COUNSEL, V15, P437
[7]   Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion [J].
Chen, CP ;
Chern, SR ;
Lee, CC ;
Chen, LF ;
Chin, DTH ;
Tzen, CY ;
Wang, W .
PRENATAL DIAGNOSIS, 2003, 23 (09) :758-761
[8]   HOLOPROSENCEPHALY IN AN INFANT WITH A MINUTE DELETION OF CHROMOSOME 21(Q223) [J].
ESTABROOKS, LL ;
RAO, KW ;
DONAHUE, RP ;
AYLSWORTH, AS .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 36 (03) :306-309
[9]  
FRYNS JP, 1987, ANN GENET-PARIS, V30, P109
[10]   Ring chromosome 15: characterization by array CGH [J].
Glass, IA ;
Rauen, KA ;
Chen, E ;
Parkes, J ;
Alberston, DG ;
Pinkel, D ;
Cotter, PD .
HUMAN GENETICS, 2006, 118 (05) :611-617