XXYY综合征的英文名字是XXYY syndrome。基因解码表明:XXYY综合征是一种染色体异常疾病,其发生与基因突变有关。 正常情况下,男性个体的性染色体组合为XY,而XXYY综合征患者则具有额外的X和Y染色体,即XXYY。这种染色体异常通常是由于精子或卵子在受精过程中发生错误,导致多余的染色体进入受精卵。 XXYY综合征的基因突变主要...
48、XXYY综合症的英文名字是48,XXYY syndrome。基因解码表明:佳学基因采用基因解码表明,48,XXYY综合症是由基因突变引起的。这种疾病是由于男性个体多拥有两个X染色体和两个Y染色体,而正常男性只有一个X染色体和一个Y染色体。这种额外的染色体是由于精子或卵子在受精过程中发生错误导致的。这种基因突变会导致一系列身体...
Related to XXYY syndrome: XXY syndromeThesaurusAntonymsRelated WordsSynonymsLegend: Switch to new thesaurus Noun 1. Klinefelter syndrome - syndrome in males that is characterized by small testes and long legs and enlarged breasts and reduced sperm production and mental retardation; a genetic defect ...
48XXYY Syndrome in an adult with type 2 diabetes mellitus, unilateral renal aplasia, and pigmentary retinitis. Case Report Med. 2010; 2010 :612315. [ PMC free article ] [ PubMed ]Zantour B, Sfar MH, Younes S, Alaya W, Kamoun M, Mkaouar E, et al. 48XXYY Syndrome in an adult ...
而对于特纳综合征（Turner's syndrome）患者来说，尽管她们的外表是女性，但由于缺少了一条X染色体，因此在巴氏小体检查中是检测不到巴氏小体的，其核型为45，XO。除此之外，还有其他一些性染色体异常的情况，例如XXY和XXYY的患者，在巴氏小体检查中会显示出一个巴氏小体，因为他们的核型中除了正常的XX...
Zhang, Qiu-ShiLi, Dong-ZhiTaylor & FrancisJournal of Maternal-Fetal MedicineZhang, Q. S., Li, D. Z., 2009. A case of 48,XXYY syndrome detected prenatally by QF-PCR. J Matern Fetal Neonatal Med. 22, 1214-6.Zhang QS, Li DZ: A case of 48, XXYY syndrome detected prenatally by QF...
48,XXYY syndrome is a sex chromosome anomaly in which males have an extra X and Y chromosome. Human cells usually contain two sex chromosomes, one from the mother and one from the father. Usually, females have two X chromosomes (XX) and males have one X and one Y chromosome (XY). ...
48XXYY Syndrome in an adult with type 2 diabetes mellitus, unilateral renal aplasia, and pigmentary retinitis. Case Report Med. 2010. [ Cross Ref ]... B Zantour,MH Sfar,S Younes,... 被引量: 2发表: 2013年 [A case of familial Bardet-Biedl syndrome (obesity, slight mental retardation,...
Analysis of developmental and behavioral characteristics of one case of XYY syndrome and one case of XXYY syndrome 在线阅读 下载PDF 引用 收藏 分享 摘要 介绍性染色体异常2例,比较其临床表现。根据行为问题、语言发育水平和社会认知水平尽早进行干预,以提高此类儿童适应学校和生活的基本能力。 In this paper,...