LD50.31
男性Klinefelter综合征，伴多于两条X染色体的
Klinefelter syndrome, male with more than two X chromosomes
- 层级
- 6 级
定义
由每个细胞中存在两个以上X染色体引起的一种影响男性的疾病。这种疾病特点是性发育受损、智力低下、典型特殊面容、骨骼异常、协调能力差以及严重的语言问题。本病可通过症状的严重程度与典型的Klinefelter综合征相鉴别。通过对两条以上X染色体进行核型分析确诊。
A disease affecting males, caused by the presence of more than two X chromosomes in each cell. This disease is characterised by impaired sexual development, intellectual disability, distinctive facial features, skeletal abnormalities, poor coordination, and severe problems with speech. This disease may be differentiated from classic Klinefelter syndrome by increased severity of symptoms. Confirmation is through observation of more than two X chromosomes by karyotyping.
索引词 可用于检索该条目的同义词与别名
- 男性Klinefelter综合征，伴多于两条X染色体的
- 男性Klinefelter综合征，伴多于两条X染色体的
- 男性Klinefelter综合征，伴多于两条X染色体
- 男性克兰费尔特综合征伴多于两条X染色体
- 男性克兰费尔特综合征，伴多于两条X染色体的
- XXXXY综合征
英文词条（4）
- Klinefelter syndrome, male with more than two X chromosomes
- male Klinefelter karyotype with more than two x chromosomes
- male Klinefelter with more than two x chromosomes
- xxxxy syndrome
后组配轴 Postcoordination
该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。