期刊文献+

1例嵌合型特纳综合征的产前诊断

下载PDF
导出
摘要 特纳综合征是一种常见的性染色体异常染色体疾病,又被称作女性先天性卵巢发育不全综合征[1]。早孕期该疾病有99%染色体单体胚胎会自然流产,活产女婴中的发病率约为1/2500[2]。特纳综合征的主要临床特征为身材矮小、颈蹼、乳头间距增宽、卵巢子宫及其他第二性征发育不良,多数患者月经异常,一般智力正常但其智力平均水平比健康同龄人低10~15分[3-4]。
出处 《国际检验医学杂志》 CAS 2023年第6期766-768,共3页 International Journal of Laboratory Medicine
基金 兰州市人才创新创业项目(2018-RC-95)。
  • 相关文献

参考文献7

二级参考文献26

  • 1Piccione M, Piro E, Serraino F, et al. Interstitial deletion of chromosome 2p15-16. 1: report of two patients and critical review of current genotype-phenotype correlation[J]. Eur J Med Genet, 2012, 55(4):238-244.
  • 2Prontera P, Bernardini L, Stangoni G, et al. Deletion 2p15-16.1 syndrome: case report and review[J]. Am J Med Genet A, 2011,155A(10) :2473-2478.
  • 3Liang JS, Shimojima K, Ohno K, et al. A newly recognised mierodeletion syndrome of 2p15-16. 1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion[J]. J Med Genet, 2009, 46(9):645-647.
  • 4Rajcan-Separovic E, Harvard C, Liu X, et al. Clinical and molecular cytogenetic characterisation of a newly recognised mierodeletion syndrome involving 2p15-16. l[J]. J Med Genet, 2007, 44(4) :269-276.
  • 5Flix TM, Petrin AI., Sanseverino MT, et al. Further characterization of microdeletion syndrome involving 2p15-p16.1 [J]- AmJ MedGenet A, 2010, 152A(10):2604-2608.
  • 6Liu X, Malenfant P, Reesor C, et al. 2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTXI and XP01 genes with autism spectrum disorders [J]. Eur J Hum Genet, 2011, 19(12):1264-1270.
  • 7Florisson JM, Mathijssen IM, Dumee B, et al. Complex craniosynostosis is associated with the 2plSp16. 1 microdeletion syndrome [J]. Am J Med Genet A, 2013, 161A(2) :244-253.
  • 8Hucthagowder V, Liu TC, Paciorkowski AR, et al. Chromosome 2p15p16. 1 microdeletion syndrome 2. 5 Mb deletion in a patient with renal anomalies, intractable seizures and a choledochal cyst[J]. Eur J Med Genet, 2012, 55(8-9):485-489.
  • 9Hancarova M, Simandlova M, Drabova J, et al. A patient with de novo 0. 45 Mb deletion of 2p16. 1: the role of BCLllA, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome [J]. Am J Med Genet A, 2013, 161A(4) :865-870.
  • 10Satterwhite E, Sonoki T, Willis TG, et al. The BCLll gene family: involvement of BCL11A in lymphoid malignancies [ J ]. Blood, 2001, 98(12):3413-3420.

共引文献238

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部