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新生儿期克氏综合征筛查:是否有依据?

Postnatal screening for Klinefelter syndrome: is there a rationale?

机构信息

Murdoch Childrens Research Institute, Parkville, Vic., Australia.

出版信息

Acta Paediatr. 2011 Jun;100(6):923-33. doi: 10.1111/j.1651-2227.2011.02151.x. Epub 2011 Feb 3.

Abstract

UNLABELLED

Diagnosis of Klinefelter syndrome (KS) allows for timely beneficial interventions across the lifespan. Most cases currently remain undiagnosed because of low awareness of KS amongst health professionals, the hesitancy of men to seek medical attention and its variable clinical presentation. Given these barriers, population-based genetic screening provides an approach to comprehensive and early detection. We examine current evidence regarding risks and benefits of diagnosing KS at different ages.

CONCLUSION

There is a lack of evidence regarding the influence of age at diagnosis on adult outcomes that can only be obtained through a pilot screening programme.

摘要

未加说明

克氏综合征(KS)的诊断可在整个生命周期内进行及时有效的干预。由于医务人员对 KS 的认识不足、男性不愿寻求医疗帮助以及其临床表现多样,大多数病例目前仍未得到诊断。鉴于这些障碍,基于人群的基因筛查为全面和早期发现提供了一种方法。我们检查了目前关于在不同年龄诊断 KS 的风险和益处的证据。

结论

关于诊断年龄对成年结果的影响,缺乏证据,只能通过试点筛查计划获得。

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