Management of epilepsy associated with tuberous sclerosis complex (TSC): Clinical recommendations

被引：122
|
作者：
Curatolo, Paolo [1 ]
Jozwiak, Sergiusz [2 ]
Nabbout, Rima [3 ]
机构：
[1] Univ Roma Tor Vergata, Dept Neurosci, Pediat Neurol Unit, I-00133 Rome, Italy
[2] Childrens Mem Hlth Inst, Dept Neurol & Epileptol, Warsaw, Poland
[3] Hop Necker Enfants Malad, Dept Neuropediat, Ctr Reference Epilepsies Rares, Paris, France
来源：
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY | 2012年 / 16卷 / 06期
关键词：
Epilepsy; Tuberous sclerosis complex (TSC); Consensus; Clinical recommendations; mTOR; VAGUS NERVE-STIMULATION; INTRACTABLE EPILEPSY; INFANTILE SPASMS; MOUSE MODEL; SEIZURES; VIGABATRIN; EVEROLIMUS; CHILDREN; SURGERY;
D O I：
10.1016/j.ejpn.2012.05.004
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Tuberous sclerosis complex (TSC) is a leading genetic cause of epilepsy. TSC-associated epilepsy generally begins during the first year of life, and is associated with neurodevelopmental and cognitive problems. Management is challenging and seizures tend to persist in a large proportion of patients despite pharmacological and surgical treatment. This report summarizes the clinical recommendations for the management of TSC-associated epilepsy made by a panel of European experts in March 2012. Current treatment options and outstanding questions are outlined. (C) 2012 Published by Elsevier Ltd on behalf of European Paediatric Neurology Society.
引用
收藏
页码：582 / 586
页数：5
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