This book offers a detailed account of all aspects of photosensitive epilepsy, including genetic testing, functional imaging (fMRI, MEG), pharmacological studies, animal studies, classification based on the occurrence of photoparoxysmal responses (PPRs) in different epilepsy syndromes, and the available prevention and treatment options. In addition, the comorbidity of and overlap between migraine and epilepsy are discussed. Informative case histories with EEG examples and a helpful glossary are included. In epilepsy, the term photosensitivity is used both for epileptic seizures triggered by flashing or flickering light and for epileptiform discharges evoked by intermittent photic stimulation (IPS) during an EEG recording. Most patients with a clear history of visually induced seizures will show epileptiform EEG discharges during IPS (PPRs). As epileptiform discharges can be evoked in photosensitive patients at any time, without triggering seizures, they can be considered a useful surrogate marker of the necessity and efficacy of epilepsy treatment. This book will serve as an ideal guide to the subject for pediatricians, (pediatric) neurologists, epileptologists, (child) psychiatrists, clinical geneticists, neuropsychologists, neuropharmacologists, occupational therapists, and basic scientists.

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.

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

The most comprehensive review of current knowledge on photosensitive epilepsy in humans. A Mac Keith Press Publication

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.

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.