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卡塔尔国家扩展代谢新生儿查计划:发生率和结果

Tala Jamaleddin1, Karen El-Akouri2,3, Sumaya Abiib1

  • 1Department of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.

International journal of neonatal screening
|July 23, 2025
PubMed
概括

卡塔尔的新生儿查检测到1:1105名婴儿的新生代谢错误 (IEM). 经典类型的homocystinuria是最常见的,突出了针对性查策略的需要.

关键词:
卡塔尔 卡塔尔 卡塔尔 卡塔尔卡塔尔国家新生儿查计划代谢过程中的先天性错误.发生率的发生率.遗传性代谢障碍 遗传性代谢障碍 遗传性代谢障碍新生儿查 新生儿查

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