Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
Eur J Neurol. 2010 Feb;17(2):179-88. doi: 10.1111/j.1468-1331.2009.02873.x. Epub 2009 Dec 28.
These EFNS guidelines on the molecular diagnosis of neurogenetic disorders are designed to provide practical help for the general neurologist to make appropriate use of molecular genetics in diagnosing neurogenetic disorders.
Literature searches were performed before expert members of the task force wrote proposals, which were discussed in detail until final consensus had been reached among all task force members.
This paper provides updated guidelines for molecular diagnosis of two particularly complex groups of disorders, the ataxias and spastic paraplegias. Possibilities and limitations of molecular genetic diagnosis of these disorders are evaluated and recommendations are provided.
本欧洲神经病学学会(EFNS)神经遗传病分子诊断指南旨在为神经科医师提供实用帮助,以使其在神经遗传病诊断中恰当运用分子遗传学。
在专家小组成员提出建议之前,进行了文献检索,之后对建议进行了详细讨论,直至小组成员达成最终共识。
本文为两种特别复杂的疾病群体(共济失调和痉挛性截瘫)的分子诊断提供了最新指南。对这些疾病的分子遗传学诊断的可能性和局限性进行了评估,并提供了相关建议。