胎儿颈部囊性淋巴管瘤的产前诊断及细胞遗传学分析
被引量：1
摘要
胎儿颈部囊性淋巴管瘤（nuchal cystic hygroma，NCH），又称囊性水瘤，是一种淋巴系统先天发育异常，主要因淋巴管发育不良、错构或受压、外伤、炎症梗阻扩张所致，是妊娠晚期流产或胎死宫内的原因之一。NCH的早期正确诊断对优生优育有重要意义。本研究回顾性分析了87例胎儿NCH的超声诊断和细胞遗传学结果，报道如下。
出处
《中华围产医学杂志》
CAS
2010年第2期134-135,共2页
Chinese Journal of Perinatal Medicine
参考文献5
-
1Makariou E, Pikis A, Harley EH. Cystic hygroma of the neck: association with a growing venous aneurysm. AJNR Am J Neuroradiol, 2003, 24: 2102-2104.
-
2Graesslin O, Derniaux E, Alanio E, et al. Characteristics and outcome of fetal cystic hygroma diagnosed in the first trimester. Acta Obstet Gynecol Scand. , 2007,86 : 1442-1446.
-
3Baena N, De Vigan C, Cariati E, et al. Prenatal detection of rare chromosomal autosomal abnormalities in Europe. Am J Med Genet A, 2003,118A:319-327.
-
4Beke A, Joo JG, Csaba A, et al. Incidence of chromosomal abnormalities in the presence of fetal subcutaneous oedema, such as nuchal oedema, cystic hygroma and non-immune hydrops. Fetal Diagn Ther, 2009,25 : 83-92.
-
5Zinn AR, Ross JL. Molecule analysis of genes on Xp controlling Turner' s syndrome premature ovarian failure (POF). Semin Reprod Med, 2001,19: 141-146.
同被引文献18
-
1Vissers LE,Veltman JA,van Kessel AG,et al. Identification of dis-ease genes by whole genome CGH arrays [ J ]. Hum Mol Genet,2005,14: R215 -R223. PMID: 16244320.
-
2Choy KW, Setlur SR, Lee C, et al. The impact of human copy num-ber variation on a new era of genetic testing [ J ]. BJOG,2010,117:391 -398. PMID:20105165.
-
3Baart EB, Martini E, Van Opstal D. Screening for aneuploidies often different chromosomes in two rounds of FISH: a short and reliableprotocol[J ]. Prenat Diagn,2004,24:955 -961. PMID: 15614916.
-
4CiriglianoV, Voglino G, Cafiadas MP,et al. Rapid prenatal diagno-sis of common chromosome aneuploidies by QF - PCR. Assessmenton 18000 consecutive clinical samplesf J ]. Mol Hum Reprod,2004,U :839 -846. PMID-.15361554.
-
5Solinas - Toldo S, et al. Matrix - based comparative genomic hybrid-ization :biochips to screen for genomic imbalances [ J ]. Genes Chro-mosomes Cancer, 1997,20- 399 - 407. PMID:9408757.
-
6TachdjianG, et al. Cryptic Xp duplication including the SHOX genein a woman with 46, X, del (X ) ( q21. 31) and premature ovarian fail-ure[J ]. Hum Reprod,2008,23:222 -6. PMID: 17981816.
-
7Portnoi'MF, Aboura A, Tachdjian G, et al. Molecular cytogeneticstudies of Xq critical regions in premature ovarian failure patients[J ]. Hum Reprod,2006,21 :2329 -34. PMID: 16751843.
-
8OlshanskayaYV, Udovichenko AI, Vodinskaya LA, et al. Myelo-dysplastic syndromes with isolated deletion of the long arm of thechromosome X as a sole cytogenetic change [J ]. Cancer Genet Cyto-genet, 2006,167:47 -50. PMID: 16682286.
-
9Chen CK, Chang SD, Chen YJ, et al. Comparative genomic hybrid-ization -^sisted prenatal diagnosis of a de novo inverted duplicationof chromosome lOq. A case report [ J ]. J Reprod Med, 2003,48 :391 -394. PMID:12815917.
-
10MiqlioriMV, Ciaschini AM, Discepoli G, et al. Distal trisomy oflOq. Report of a new case of duplication 10q25. 2 -25. 3 —?qter de-fined by FISH[J ]. Ann Genet, 2002,45:9 - 12. PMID; 11934383.
二级引证文献2
-
1黄伟伟,卢建,杨曦,陈秋平,刘舒,尹爱华.微阵列在22q11.2微缺失综合征诊断和产前诊断中的应用[J].河南科技大学学报（医学版）,2015,33(3):164-165. 被引量：2
-
2王坦,蔺春茂,尹焕才,殷建.21-三体综合征产前筛查及诊断技术的研究进展[J].中国科学：生命科学,2024,54(7):1173-1182.
-
1刘莹.彩超诊断多胎妊娠合并联体双胎1例[J].中国医学影像技术,2003,19(7):914-914.
-
2杜娟,曲陆荣,郭淑香.B超诊断胎儿颈部囊性淋巴管瘤22例分析[J].中华妇产科杂志,1997,32(7):425-427. 被引量：12
-
3蒋银花,唐毅,赵斌.B超诊断胎儿颈部囊性淋巴管瘤2例[J].西北国防医学杂志,2002,23(4):264-264.
-
4苏陈艾,娣丽努尔.B超对胎儿淋巴系统畸形的诊断[J].新疆医学,2006,36(2):136-138.
-
5杜娟,高嵩.胎儿颈部囊性淋巴管瘤的产前诊断与预后[J].中国实用妇科与产科杂志,2000,16(5):278-278.
-
6董宁宁,张砚芳.B超诊断胎儿囊性水瘤畸形1例[J].沈阳部队医药,1998,11(2):130-130.
-
7马金凤,罗玲斐.68例宫颈功能不全的疗效观察[J].现代中西医结合杂志,2008,17(20):3107-3108. 被引量：7
-
8申雅琳.宫颈机能不全43例临床分析[J].中国实用医药,2012,7(10):129-130.
-
9张霞.宫颈机能不全37例探讨[J].健康大视野（医学版）,2014,22(2):69-70. 被引量：3
-
10范美玲.宫颈环扎术治疗宫颈机能不全应用效果[J].医疗装备,2016,29(2):91-92.
