Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy

被引:14
作者
Chen, Chih-Ping [1 ,2 ,3 ,4 ,5 ,6 ]
Su, Yi-Ning [7 ]
Hsu, Chin-Yuan [1 ]
Chern, Schu-Rern [2 ]
Lee, Chen-Chi [1 ]
Chen, Yu-Ting [2 ]
Chen, Wen-Lin [1 ]
Wang, Wayseen [2 ,8 ]
机构
[1] Mackay Mem Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[2] Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan
[3] Asia Univ, Dept Biotechnol, Taichung, Taiwan
[4] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung, Taiwan
[5] Natl Yang Ming Univ, Inst Clin & Community Hlth Nursing, Taipei 112, Taiwan
[6] Natl Yang Ming Univ, Sch Med, Dept Obstet & Gynecol, Taipei 112, Taiwan
[7] Natl Taiwan Univ Hosp, Dept Med Genet, Taipei, Taiwan
[8] Tatung Univ, Dept Bioengn, Taipei 104, Taiwan
来源
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | 2011年 / 50卷 / 04期
关键词
3p deletion; 3q duplication; CHL1; Deletion-duplication syndrome of chromosome 3; Fetoplacental discrepancy; Mosaicism; PARTIAL TRISOMY 3Q; SHORT ARM; PERICENTRIC-INVERSION; MENTAL-RETARDATION; TERMINAL DELETION; PURE DUPLICATION; DUP(3Q) SYNDROME; DISTAL DELETION; DELINEATION; KARYOTYPE;
D O I
10.1016/j.tjog.2011.10.015
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To present prenatal molecular cytogenetic diagnosis of mosaicism for terminal 3p deletion and distal 3q duplication using cultured and uncultured amniocytes, and the association with fetoplacental discrepancy. Materials, Methods, and Results: A 35-year-old primigravid woman was referred for genetic counseling at 21 weeks of gestation because of 20% (5/25 colonies) mosaicism for add(3)(p26) detected by amniocentesis. Repeated amniocenteses were performed. Array comparative genomic hybridization (aCGH) and interphase fluorescence in situ hybridization (FISH) were applied in the uncultured amniocytes. aCGH analysis detected 0.15-Mb microdeletion of 3p26.3 with CHL1 haploinsufticiency and a 49.42-Mb duplication of 3q24-q29 in the uncultured amniocytes. Interphase FISH analysis revealed 27.3% mosaicism (12/44 cells) in the uncultured amniocytes. Metaphase FISH analysis revealed 23.3% mosaicism (7/30 cells) in the cultured amniocytes. Conventional cytogenetic analysis showed a karyotype of 46,XX,der(3)(qter -> q24::p26.3 -> qter)[10]/46,XX[20] (33% mosaicism). Subsequent fetal blood sampling showed a karyotype of 46,XX,der(3) (qter -> q24::p26.3 -> qter)[5]/46,XX[35] (12.5% mosaicism). The parents elected to terminate the pregnancy, and a malformed fetus was delivered at 24 weeks of gestation with characteristic facial dysmorphism and clinodactyly of the hands. Cytogenetic analysis of the extra-embryonic tissues revealed the results of 46,XX (40 cells) in placenta, 25% mosaicism (10/40 cells) in amniotic membrane and 50% mosaicism (20/40 cells) in umbilical cord. Conclusion: Our presentation highlights the utility of molecular cytogenetic technologies in prenatal diagnosis of rare mosaic chromosome rearrangements and provides evidence for fetoplacental discrepancy under such circumstances. Copyright (C) 2011, Taiwan Association of Obstetrics & Gynecology. Published by Elsevier Taiwan LLC. All rights reserved.
引用
收藏
页码:485 / 491
页数:7
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