This book gives an exhaustive account of the classification and management of epileptic disorders. It provides clear didactic guidance on the diagnosis and treatment of epileptic syndromes and seizures through thirteen chapters, complemented by a pharmacopoeia and CD ROM of video-EEGs.

This title will be an exhaustive and thorough text on the range of epileptic conditions, aiming to be the standard reference text on epilepsies for neurologists. It presents established views and recent advances in epileptic seizures and syndromes and their management, and the content is based on the classification, practice parameters and guidelines issued by the International League Against Epilepsy and other recognised medical authorities.

Expanded and revised, this unique book provides concise descriptions of the many causes of epilepsy, for use in clinical practice.

Reflex epilepsies can provide a qualitative and quantitative viewpoint of the complexities of ictogenesis. The various chapters in this book examine the factors that can trigger a seizure, such as hot water, food, contact and movement, music and emotions. The relationship between several reflex epilepsy mechanisms and juvenile myoclonic epilepsy is discussed along with the significance of their occurrence in syndromes, enhancing our understanding of current epilepsy nosology. The conventional dichotomy appears outdated, while functional studies of trigger mechanisms are moving more towards central nervous system subsets acting as pathological networks that produce seizures in generalized and focal epilepsies.

Covers all aspects of epilepsy, from basic mechanisms to diagnosis and management, as well as legal and social considerations.

Eyelid myoclonia with absences is a recently described and under-recognised syndrome of idiopathic generalised epilepsy. The diagnosis may be confused with tics, attempts at self induction, and epilepsy syndromes with a better prognosis such as childhood absence epilepsy. This book summarises current knowledge on the topic; covering the underlying anatomy and physiology of the eyelids, the clinical and electro-encephalographic features and differential diagnosis in children and adults, including a discussion on the issue of self-induction of absences. The current state of knowledge on inheritance and genetics of the condition and treatment strategies are considered. Throughout, recent advances in the field are couched in an historical context, making this book a comprehensive source for all those who need to understand this syndrome whether from a research standpoint or the clinical management of affected children and adults. As such it will be of value to neurologists, epileptologists and those involved in the care and treatment of epileptic patients.

Affecting 4 percent of children and 1-2 percent of the general population, epilepsy is one of the most common neurological disorders. The 1st edition of this guide proved to be the only one of its kind, covering many important aspects of diagnosis and treatment. Due to the continued advances being made in the subject, and building on the sell-out success of the 1st edition this thorough revision reflects the latest report of the ILAE classification core group and the significant progress made in the diagnosis, classification and treatment of the epilepsies.