论文部分内容阅读
新生儿疾病筛查是遗传代谢缺陷病的一种早期诊断和早期防治方法,其根本在于对检出的遗传代谢缺乏进行治疗。其是儿童保健的重要组成部分,是提高出生人口素质的有效措施之一。江西省从1997年10月份起开展新生儿疾病筛查工作,10年来取得了一定成绩,但还存在不足,有待于加强与完善
Neonatal disease screening is an early diagnosis and early prevention and treatment of genetic metabolic deficiency disease, which is based on the detection of the lack of genetic metabolic treatment. It is an important component of child health and is one of the effective measures to improve the quality of the born population. Since October 1997, Jiangxi Province has carried out screening of neonatal diseases, and some achievements have been made in the past 10 years, but there are still some deficiencies that need to be strengthened and perfected