Suppr超能文献

同型胱氨酸尿症的出生患病率。

Birth prevalence of homocystinuria.

作者信息

Refsum Helga, Fredriksen Ase, Meyer Klaus, Ueland Per M, Kase Bengt Frode

机构信息

Department of Pharmacology, University of Oxford, United Kingdom.

出版信息

J Pediatr. 2004 Jun;144(6):830-2. doi: 10.1016/j.jpeds.2004.03.004.

Abstract

Serious complications of homocystinuria caused by cystathionine beta-synthase deficiency can be prevented by early intervention. We determined the prevalence of 6 specific mutations in 1133 newborn blood samples. Our results suggest that homocystinuria is more common than previously reported. Newborn screening for homocystinuria through mutation detection should be further considered.

摘要

由胱硫醚β-合酶缺乏引起的同型胱氨酸尿症的严重并发症可通过早期干预预防。我们测定了1133份新生儿血样中6种特定突变的发生率。我们的结果表明,同型胱氨酸尿症比之前报道的更为常见。应进一步考虑通过突变检测对同型胱氨酸尿症进行新生儿筛查。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验