摘要
本文报道上海地区14个单位从1981年10月~1982年9月,对31,861名新生儿进行三种代谢病的筛查。结果:18,926名中检到先天性甲状腺功能减退者3例,检出率为1/6,309;31,861名中检到苯丙酮尿症者2例,检出率为1/15,930;31,861名中筛查半乳糖血症均未检到阳性病例。另对有关筛查方法、诊断及其重要意义进行讨论。
A total number of 31,861 neonates from 14 hospitals in Shanghai was screened for hypothyroidism, phenylketonuria and 8alactosemia from Oct 1981 to Sept 1982. Three cases of hypothyroidism were demonstrated in 18,926 neonates, the detection rate being1/6,309. Two cases of phenylkconuria were proved in 31,861, the detection rate being1/15,930. No case of galactoscmia was identified in 31,861. The screening technique, diagnosis and significance of this study are briefly discussed.
出处
《上海医学》
CAS
1983年第6期344-347,共4页
Shanghai Medical Journal
