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Lennox-Gastaut syndrome: a comprehensive review.

Author: Asadi-PooyaAli A

Journal ArticleAn article published in an academic or professional journal that reports original research or scholarly analysis.
ReviewAn article that critically examines existing research on a particular topic and summarizes the current state of knowledge in the field.

Overview

Lennox-Gastaut syndrome (LGS) is a severe epilepsy characterized by drug-resistant seizures, specific EEG patterns, and intellectual disability. The treatment aims to reduce the frequency of the most debilitating seizures. Valproate, lamotrigine, and topiramate are considered first-line treatments, while other options include levetiracetam, clobazam, rufinamide, and zonisamide.
Paper Details　
Original Abstract of the Article :
Lennox-Gastaut syndrome (LGS) is considered an epileptic encephalopathy and is defined by a triad of multiple drug-resistant seizure types, a specific EEG pattern showing bursts of slow spike-wave complexes or generalized paroxysmal fast activity, and intellectual disability. The prevalence of LGS i...See full text at original site
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引用元：
https://doi.org/10.1007/s10072-017-3188-y

データ提供：米国国立医学図書館（NLM）

Lennox-Gastaut Syndrome: A Complex and Challenging Epilepsy

Lennox-Gastaut syndrome (LGS), a severe form of epilepsy, presents a significant challenge for patients and clinicians. This review provides a comprehensive overview of LGS, covering its [etiology, clinical features, diagnosis, treatment options, and long-term outcomes]. The authors delve into the diverse causes of LGS, highlighting the challenges associated with managing this complex neurological disorder. This review serves as a valuable resource for understanding LGS and exploring available treatment strategies.

Navigating the Intricacies of LGS: A Guide for Clinicians

This comprehensive review provides a detailed exploration of [Lennox-Gastaut syndrome (LGS)], a complex and challenging form of epilepsy. The authors systematically review the current understanding of LGS, covering its [etiology, clinical features, diagnosis, treatment options, and long-term outcomes]. This review serves as a valuable resource for clinicians seeking to understand and manage this complex neurological disorder.

Living with LGS: A Journey of Hope and Resilience

LGS can significantly impact the lives of patients, affecting their [cognitive abilities, physical function, and overall quality of life]. This review highlights the importance of a [multidisciplinary approach] to managing LGS, involving a team of specialists to address the diverse needs of patients. While the long-term prognosis for LGS can be challenging, ongoing research and advancements in treatment strategies offer hope for improving the lives of individuals affected by this condition.

Dr.Camel's Conclusion

This review explores the complex world of Lennox-Gastaut syndrome (LGS), providing a comprehensive guide for understanding and managing this challenging neurological disorder. Think of LGS as a desert landscape: it's vast, complex, and often unpredictable. Just as desert nomads must navigate their environment with skill and resourcefulness, so too must clinicians approach LGS with a multidisciplinary approach and unwavering commitment to improving the lives of their patients. This research provides a roadmap for navigating the intricacies of LGS, offering valuable insights and fostering hope for those seeking effective treatment strategies.

Date :
  1. Date Completed 2018-08-30
  2. Date Revised 2018-11-13
Further Info :

Pubmed ID

29124439

DOI: Digital Object Identifier

10.1007/s10072-017-3188-y

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Languages

English

Positive IndicatorAn AI analysis index that serves as a benchmark for how positive the results of the study are. Note that it is a benchmark and requires careful interpretation and consideration of different perspectives.

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