Neurocutaneous Syndromes provides the most updated and comprehensive resource on the disorders that lead to the growth of tumors in various parts of the body, those caused by the abnormal development of cells in an embryo and characterized by the presence of tumors in various parts of the body and eyes, including the nervous system, and by certain differences in the skin. The most common neurocutaneous syndromes include, neurofibromatosis, Sturge-Weber syndrome, tuberous sclerosis, ataxia-telangiectasia, and von Hippel-Lindau disease. Symptoms vary widely and while present early may not express until later in life. As molecular medicine and genetic science is continuing to impact our understanding of neurocutaneous syndromes, this book also includes the latest molecular and genetic science.

Manual of Pediatric Neurology is an easy-to-read and easy-to-access text based on clinical scenarios. Emphasis is placed on signs and symptoms, diagnostic tests as needed, and practical advice on treatment for childhood neurologic disorders. The book comprises a collection of chapters that address frequently encountered pediatric scenarios in all clinical settings. These include the management of seizures in the emergency department, treatment of epilepsy in the outpatient setting, acute management of headaches and many more. The book also covers topics juxtaposed to neurology such as neonatal neurology, neurogenetics, and the management of stroke in children. Special attention is placed on commonly encountered neurological conditions such as Tourette' syndrome, neuromuscular illnesses, and CNS infections. Interpretation of frequently used tests such as EEG, CSF analysis, and nerve conduction testing is also covered. Finally, one chapter is devoted to the care of child neurology patients at the end of life, i.e. palliative care.

Sturge-Weber syndrome is an enigmatic disorder, seldom difficult to diagnose but often difficult to treat. This book consolidates what is known about the Sturge-Weber syndrome in the hope that this information will be useful in the care of patients and serve as a stimulus to encourage research on some of the remaining questions about the syndrome.This book is the 2nd Edition. The 1st Edition was published in June 1999, ISBN-10: 0967048400; ISBN 13: 978-0967048406