A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.
摘要作者例具有多种先
性异常
三染色体22症
活产女婴。
A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.
摘要作者例具有多种先
性异常
三染色体22症
活产女婴。
*X represents monosomy 21,diploid,trisomy 21,tetrasonmy 21 and hexasomy 21 in the corresponding box.
(X代表相应栏中21单体、二倍体、21三体、四体和六体);
Polysomy, which includes trisomy, is the condition in which one or more chromosomes are represented more than twice in the cell.
多染色体包括三染色体都是条或多条染色体代替了正常细胞中
两条染色体形成
。
So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.
这样,本例儿显示21三体
若干征象:包括鼻骨发育不全、牙发育不全、小颌和尿道下裂。
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