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47,XYY综合征一例 被引量：2

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摘要 47,XYY综合征（超雄综合征）是一种性染色体异常综合征,在成年男性中报道较少,近日我所诊断一例47,XYY综合征,现将此病例报道如下。
作者 余小英 何淑凤 徐庆阳 王玉萍 彭弋峰
机构地区 皖南医学院弋矶山医院生殖医学研究所 皖南医学院弋矶山医院检验科遗传室
出处 《中国优生与遗传杂志》 2012年第3期59-59,共1页 Chinese Journal of Birth Health & Heredity
关键词 XYY综合征 染色体异常综合征 超雄综合征 病例报道
分类号 R596 [医药卫生—内科学]
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参考文献2

二级参考文献9

  • 1Shanske A, Sachmechi I, Patel DK, et al. An adult with 49, XYYYY karyotype:case report and endocrine studies[J]. Am J Med Genet, 1998 Nov 2,80(2) : 103 - 106,.
  • 2Buyse ME, ed, Chromosome X, chromosome XYY, In:Birth Defects Encyclopedia[M].Cambridge, Massachusetts: Blackwell Scientific Publications,1990.400-401.
  • 3Linden MG, Bender BG, Robinson A. Intrauterine diagnosis of sex chromosome aneuploidy[J]. Obstet Gynecol, 1996,87:468 - 475.
  • 4Das GP,Shukla A, Verma IC. Phenotype of 49, XYYYY[J]. Clin Genet,1993,43:196- 199.
  • 5Ferguson- Smith MA, Yates JR. Materna age specific rotes for chromosome aberrations and factors influencing them:report of a collaborative European study on 52965 amniocenteses[J]. Prenat Diagn, 1984,4:5 - 44.
  • 6Martin RH,Shi Q, Field LL. Recombination in the pseudoautosomal region in a 47 ,XYY male[J]. Hum Genet,2001 Aug, 109(2) : 143 - 145.
  • 7Shi Q, Martin RH. Multicolor fluorescence in situ hybidization analysis of meiotic chromosome segregation in a 47, XYY male and a review of the literature[J]. Am J Med Genet,2000 Jul 3,93(1):40-46.
  • 8Martin RH, McInnes B, Rademaker AW. Analysis of aneuploidy for chromosome 13.21, X and Y by multicolour fluorescence in situ hybridization (FISH) in a 47, XYY male[J]. Zygote. 1999, 7 : 131 - 134.
  • 9Blanco J, Rubio C, Simon C, et al. Increased incidence of disomic sperm nuclei in a 47, XYY male assessed by fluorescent in situ hybrization (FISH)[J]. Hum Genet, 1997,99:413 - 416.

共引文献8

同被引文献29

  • 1朱春业.男性性染色体异常与犯罪[J].大家健康,1995,0(8):36-36. 被引量：1
  • 2Sandberg AA, Koepf GF, Ishihara T, et al. An XYY human male[J]. Lancet, 1961,2:448.
  • 3Grouchy JD, Tudeau C. Atlas of Human Chromosomes[M].lsted. New York :John Wiley, 1977.248.
  • 4Lindan MG, Bender BG, Robinson A. Intrauterine diagnosis of sex chromosome aneuploidy[J].Obstet Gynecol, 1996,87 (3) :468-475.
  • 5Faeza El-Dahtory, Hany M Elsheikha. Male infertility related to an aberrant karyotype, 47,XYY :four case reports[J].Cases J, 2009,2 (1) :28.
  • 6王国良译,谈湧布,张忠恕校.47,XYY父亲的异常小孩[J].国外医学遗传学分册,1980,4:222-223.
  • 7Blanco J, Egozcue J, Vidal F. Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47,XXY, mosaic 46,XY/47,XXY and 47,XYY)assessed by fluorescence in situ hybridization [J].Hum Reprod, 2001, 16 : 887-892.
  • 8Martin RH, Shi Q, Field LL. Recombination in the pseudoautosomal region in a 47,XYY male[J].Hum Genet, 2001,109 (2) :143-145.
  • 9Shi Q, Martin RH. Multicolor fluorescence in situ hybridization analysis of meiotic chromosome segregation in a 47,XYY male and a review of the literature[J].Am J Med Genet, 2000, 03 ( 1 ) :40-46.
  • 10Jordi Benet, Renee H. Martin. Sperm chromosome complement in a 47,XYY man[J].Human Genetics, 1988, 78 (4) : 313-315.

引证文献2

二级引证文献13

中国优生与遗传杂志
2012年 第3期

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