Lennox–Gastaut syndrome (LGS), a severe childhood-onset epilepsy syndrome, can be challenging to identify due to its heterogeneous presentation. This article summarised interviews conducted with Karen C. Keough, Texas A&M University School of Medicine, USA, and Rhys H. Thomas, Royal Victoria Infirmary and Newcastle University, UK, who explored the challenges in diagnosing LGS.
In this issue
Rate this content's potential impact on patient outcomes
Thank you!
Please share some more information on the rating you have given