So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.
这样，本例胎儿显21的若干征象：括鼻骨发育、发育、小颌和尿道下裂。
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The cerebellum can also be smaller in size, called cerebellar hypoplasia, leading to trouble with movement and balance.
患儿的也可能偏，称作“发育不全”，会导和维持身体平衡方面的障碍。
After about two weeks in the NICU, they informed us that Bella had a very rare genetic disorder called Pontocerebellar hypoplasia, type 6.
在新生儿重症监护病房约两周后，他们告诉我们贝拉患有一种非常罕见的遗传性疾病，叫做发育不全，6型。
This beta cell compensation, though, isn't sustainable, and over time those maxed out beta cells get exhausted, and they become dysfunctional, and undergo hypotrophy and get smaller, as well as hypoplasia and die off.
然而β细胞增益不能长久维持，久而久之，那些肥的β细胞会疲劳，出现功能障碍，而且细胞开始萎缩变，同时细胞减少，相继死亡。
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划词翻译
详细解释
21
的若干征象：
括鼻骨发育
、
发育
也可能偏
和维持身体平衡方面的障碍。
约两周后，他们告诉我们贝拉患有一种非常罕见的遗传性疾病，叫做
