产前超声诊断Beckwith—Wiedemann综合征一例
摘要
孕妇27岁,停经32周,孕1产0。平素月经规律,周期5/23d,末次月经2008年10月12日,预产期2009年7月19口,核对预产期准确。唐氏筛查低危,50g葡萄糖负荷试验7.6mmol/L。停经22周超声提示中孕活胎,未见明显异常。
出处
《中华围产医学杂志》
CAS
2010年第3期259-260,共2页
Chinese Journal of Perinatal Medicine
基金
国家科技部支撑计划“重大出生缺陷和遗传病的防治研究-严重胎儿结构异常影像学产前筛查和诊断新技术的研究”(2006BA105A04)
参考文献4
-
1Weksberg R,Shuman C,Beckwith JB.Beekwith-Wiedemanr syndrome.Eur J Hum Genet,2009,18:8-14.
-
2朱喜科,路平,卢岩,邵阳阳.巨大舌-脐膨出综合征与基因组印记[J].中华医学遗传学杂志,2002,19(1):79-81. 被引量:4
-
3Chen CP.Syndrome and disorders associated with omphalocele (I):Beckwith-Wiedemann syndrome.Taiwan J Obstet Gynecol,2007,46:96-102.
-
4O'Connor C,Levine D.Case 49:Beckwith-Wiedemann syndrome.Radiology,2002,224:375-378.
二级参考文献29
-
1Mannens M, Hoovers JMN, Redeker E, et al.Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckhwith-Wiedemann syndrome and various human neoplasia. Eur J Hum Genet, 1994,2∶3-23.
-
2Lalande M. Parental imprinting and human disease. Annu Rev Genet, 1996,30∶173-195.
-
3Junien C. Beckwith-Wiedemann syndrome, tumorigenesis and imprinting. Curr Opin Genet Dev, 1992,2∶431-438.
-
4Henry I, Bonaiti-Pelle C, Chehensse V, et al. Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature, 1991,351∶665-667.
-
5Ping AJ, Reeve AE, Law DJ, et al. Genetic linkage of Beckwith-Wiedemann syndrome. Am J Hum Genet, 1989,44∶720-723.
-
6Koufos A, Grundy P, Morgan K, et al. Familial Beckwith-Wiedemann syndrome and a second Wilms tumor locus both map to 11p15.5. Am J Hum Genet,1989,44∶711-719.
-
7Zhu X, Higashimoto K, Soejima H, et al. C11 or f21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5. Gene,2000,256∶311-317.
-
8Matsuoka S, Edwards MC, Bai C, et al.p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. Genes Dev, 1995,9∶650-662.
-
9Hatada I, Mukai T. Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse. Nat Genet, 1995,11∶204-206.
-
10Hatada I, Inazawa J, Abe T, et al. Genomic imprinting of human p57KIP2 and its reduced expression in Wilm's tumor. Hum Mol Genet, 1996,5∶783-788.
共引文献3
-
1张春兰,任秀艳.哺乳动物的基因组印记与印记基因疾病[J].潍坊学院学报,2004,4(2):23-24.
-
2李有贵,张作法,时连根.IGF2基因的遗传学特征与生物学意义[J].科技通报,2005,21(4):396-399. 被引量:1
-
3朱婵,徐勇飞,渠利利,王书奎.IGF2的生物学特性及其与疾病关系的研究进展[J].国际检验医学杂志,2010,31(9):966-969. 被引量:15
-
1丛翔,展新风,程琳,王音,陶国伟,罗霞,刘韶平.产前超声诊断Beckwith—Wiedemann综合征1例[J].中华超声影像学杂志,2013,22(9):819-819. 被引量:3
-
2李晶晶,宋红,宋焕清.试管婴儿双胎之一患Beckwith-Wiedemann综合征1例报告[J].山东医药,2013,53(31):107-108. 被引量:2
-
3梁红,王庆杰,陈净,郭静.Beckwith-Wiedemann综合征一例[J].中华儿科杂志,2005,43(12):945-946. 被引量:3
-
4孙碧君,程国强,吴冰冰,杨琳,王来栓,曹云,陈超,周文浩.体外受精-胚胎移植受孕双胎之一Beckwith-Wiedemann综合征一例[J].中华围产医学杂志,2015,18(4):301-304. 被引量:1
-
5沈卫民,崔杰,陈建兵,季易,陈海妮,邹继军.Beckwith-Wiedemann综合征一例[J].中华整形外科杂志,2012,28(1):72-74. 被引量:1
-
6黄强,王建六.停经29^(+4)周,头晕、头痛伴眼花4d[J].山东医药,2010,50(40):114-115.
-
7陆桂香,石霖.Beckwith-Wiedemann综合征1例报告[J].中国优生与遗传杂志,2002,10(2):58-58.
-
8李娜,李朝霞.产前出血、血管前置并死胎1例及文献复习[J].中国临床研究,2013,26(5):478-479.
-
9杨昆霖,范丽欣,杨慧霞,孙伟杰,时春艳,刘喆,胡君,张阳阳,徐海燕.产前诊断胎盘植入伴血管前置一例[J].中华围产医学杂志,2014,17(3):216-217. 被引量:3
-
10曹小丽,石磊,王丽,刘瑞华,姜宏.胎儿Beckwith—Wiedemann综合征超声表现1例[J].中华超声影像学杂志,2007,16(6):480-480.