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...
因此,基因检测可以增加48,XXYY综合症的诊断正确性,并为患者提供更好的医疗管理和护理。 48、XXYY综合症(48,XXYY syndrome)采用全外显子测序基因解码技术为什么会减少误诊的可能性 48、XXYY综合症是一种由佳学基因检测进行检测与分析染色体异常疾病,其特征是男性患者具有两个额外的性染色体,即XXYY。这种疾病的确诊通常...
48,XXYY syndromeis asex chromosome aneuploidy(SCA) condition that occurs in approximately 1:18000 to 1:40000 males.Developmental delaysand behavioral problems are the most common reason for genetic testing. The physical phenotype of 48,XXYY is similar to 47,XXYKlinefelter syndrome(tall stature,hyper...
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 ...
XXYY syndromeChromosome disorderAbnormal genitaliaThe XXYY syndrome, an uncommon disorder of chromosome number, was discovered on routine physical examination of a 20-year-old patient. Despite numerous earlier contacts with physicians, including several visits during adolescence, insufficient consideration had...
参考 ^THE "DOUBLE MALE": A NEW CHROMOSOME CONSTITUTION IN KLINEFELTER'S SYNDROME Muldal, S. et...
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, 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-PCR. J Matern Fetal Neonatal Med 2009, 22 (12) : 1214–1216....
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...