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[优化罕见病患者的治疗]

[Optimising treatment for people with rare diseases].

作者信息

Lund Allan Meldgaard, Skovby Flemming

机构信息

H:S Rigshospitalet, Juliane Marie Centret, Klinisk Genetisk Afdeling, København Ø.

出版信息

Ugeskr Laeger. 2006 Apr 10;168(15):1547-50.

Abstract

Diagnosis of and care for people with rare diseases are a challenge. Most rare diseases are inherited with clinical presentation in early childhood, complex with involvement of several organ systems and progressive with ever changing phenotype. Physical and neurological disability makes many families dependent on social security. In Denmark and in a few other EU countries, centres of reference for the care of people with rare diseases have been established. The impression is that the effect of establishing such centres for these rare diseases in Denmark has been good and that it remains the most rational way of treatment.

摘要

罕见病患者的诊断和护理是一项挑战。大多数罕见病是遗传性的,在儿童早期出现临床表现,病情复杂,累及多个器官系统,且表型不断变化。身体和神经残疾使许多家庭依赖社会保障。在丹麦和其他一些欧盟国家,已经设立了罕见病患者护理参考中心。给人的印象是,在丹麦为这些罕见病设立此类中心的效果很好,而且这仍然是最合理的治疗方式。

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