目的探讨分析儿童矮小症的病因及误诊原因。
Objective To investigate the etiology and misdiagnosis of microsomia children.
用于诊断高血压、体重超重、肥胖、消瘦、矮小症。
For the diagnosis of hypertension, overweight, obesity, weight loss, Dwarf.
但是据报告说，青少年患有先天矮小症，通常这能使平均寿命减少至少20年。
But reports say that the teenager suffers from primordial dwarfism, a condition that typically reduces life expectancy to as little as 20 years.
艾比得了一种非常罕见的先天性不对称身材矮小性发育异综合征，又称原始侏儒症，发病率只有十万分之一。
She suffers from a very rare genetic condition called Russell-Silver syndrome, a form of primordial dwarfism which affects only one in 100,000 babies.
艾比得了一种非常罕见的先天性不对称身材矮小性发育异综合征，又称原始侏儒症，发病率只有十万分之一。
She suffers from a very rare genetic condition called Russell-Silver syndrome a form of primordial dwarfism which affects only one in 100000 babies.
努南综合症被定义为一种常染色体显性的遗传性综合症，其一般特征为身材矮小、先天性心脏缺损、以及独特的面部特征。
Noonan syndrome is defined as an autosomal dominant genetic syndrome commonly characterized by short stature, congenital heart defects, and unique facial features.
努南综合症被定义为一种常染色体显性的遗传性综合症，其一般特征为身材矮小、先天性心脏缺损、以及独特的面部特征。
Noonan syndrome is defined as an autosomal dominant genetic syndrome commonly characterized by short stature, congenital heart defects, and unique facial features.
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