Inherited Metabolic Epilepsies

Double click on above image to view full picture

Zoom Out
Zoom In

Inherited Metabolic Epilepsies

SKU# 9781936287253

Author: Phillip L. Pearl MD

$99.00

Other Vendors:

Amazon | Barnes & Noble

Description

The explosion of information in neurogenetics and metabolism mandates increasing awareness of appropriate diagnostic and therapeutic strategies in the setting of certain epilepsies, especially those of very early onset. There are over 200 inherited disorders that are associated with seizures and prompt identification and intervention is crucial for a positive outcome. This text brings together leading authorities presenting state-of-the-art clinical reviews covering the science, recognition, and treatment of the inherited metabolic epilepsies and related disorders.

Inherited Metabolic Epilepsies opens with a section on general principles for diagnosis and targeted intervention including screening protocols, laboratory testing, neuroimaging, seizure patterns and EEG findings, new technologies, and the ketogenic diet in metabolic epilepsies. The next two sections are devoted to the cohort of specific small molecule disorders (aminoacidopathies, organic acidopathies, mitochondrial disorders, urea cycle disorders, neurotransmitter disorders, and glucose-related disorders) and large molecule disorders (lysomal storage disorders, peroxisomal diseases, glycosylation defects, and leukodystrophies) that are treatable yet can be so vexing to clinicians and investigators. The book concludes with a clinical algorithm designed to be a resource for the physician in search of direction when considering an inherited metabolic disorder as the explanation for a patient with epilepsy.

Inherited Metabolic Epilepsies Key Features:

  • Presents the latest scientific thinking and clinical wisdom for a poorly understood group of disorders that have devastating consequences if unrecognized or not promptly treated
  • Expert authorship from both the genetic-metabolic and epilepsy communities provides state-of-the-art guidance for understanding and managing these disorders
  • A readable text for clinicians highlighting the relation between metabolic errors and epilepsy
  • Concludes with a practical algorithm for evaluating a patient with a possible metabolic epilepsy

Product Details

  • Publication Date October 04, 2012
  • Page Count 376
  • Product Form Hardback
  • ISBN 13 9781936287253
  • EISBN 9781617050565

Editorial Review(s)

This book fills an important and unique niche in pediatric neurology, and will be a frequently referenced textbook for all clinicians caring for children with epilepsy." - Neurology, August 2013

About The Author(s)

Phillip L. Pearl
Philip L. Pearl, MD, is Chief of the Division of Neurology at Children's National Medical Center and Professor of Neurology, Pediatrics, and Music at The George Washington University School of Medicine and Columbian College of Arts and Sciences, Washington, DC

Table of Contents

Forward: Inherited Metabolic Epilepsies: Diagnostic Challenges, Treatable Entities, and New Frontiers, Phillip L. Pearl; I. General Principles: 1. Treatable Metabolic Epilepsies: The Top Ten Diagnoses You Can't Afford to Miss, Phillip L. Pearl; 2. Neuroimaging in the Metabolic Epilepsies, Zarir P. Khademian and Robert Zimmerman; 3. Advances in MR Spectroscopy for Inherited Epilepsies, Andrea Gropman, Andrew Breeden, and Morgan Prust; 4. Electroencephalography in the Metabolic Epilepsies, Mona Al-Dulaligan and Phillip L. Pearl; 5. Genetic Counseling in the Metabolic Epilepsies, Jodie Martin; 6. Ketogenic Diet in Metabolic Epilepsies, Eric H. W. Kossoff; II. Small Molecule Diseases: 7. Amino and Organic Acid Disorders and Epilepsy, Kimberly Chapman; 8. Fatty Acid Oxidation Disorders and Epilepsy, Dieter Matern and Dimitar Gavrilov; 9. Urea Cycle Disorders and Epilepsy, Marshall Summar, Brendan Lanpher, and Debra Regier; 10. Mitochondrial Diseases and Epilepsy, Andrea Gropman, Sumit Parikh, and Lynn Wolfe; 11. Vitamin B6 Responsive Seizures in All Its Forms: Pyridoxine, Pyridoxal-5-Phosphate, and Folinic Acid Dependency, Sidney M. Gospe, Jr.;12. Tetrahydrobiopterin Deficiencies and Epilepsy, Nenad Blau and Thomas Opladen; 13. Disorders of GABA Metabolism and Epilepsy, Phillip L. Pearl, K. Michael Gibson, and Cornelius Jakobs; 14. Glucose Transporter Type 1 Deficiency Syndrome, From Inception to Future Directions, Darryl C. De Vivo and Amanda Pong; 15. Developmental Delay, Epilepsy, and Neonatal Diabetes (DEND), A Potassium Channelopathy Leading to Epilepsy, Frances Ashcroft and Carolina Lahmann; 16. Hyperinsulinsm/Hyperammonemia (HI/HA) and Epilepsy, Andrea Kelly and Nicholas S. Abend; 17. Glycine Encephalopathy and Epilepsy, Julia B. Hennermann; 18. Serine Synthesis Defects and Epilepsy, T. De Koning; 19. Lesch-Nyhan Disease and Epilepsy, Hal Jinnah and Beth A. Leeman; 20. Sulfite Oxidase/Mb Cofactor Deficiency and Epilepsy, Joern Sass and Barbara Plecko-Startinig; 21. Creatine Disorders and Epilepsy, Ton DeGrauw; 22. Cerebral Folate Deficiency and Epilepsy, Fernando Scaglia; 23. Homocysteinemias and Epilepsy, William M. McClintock; III. Large Molecule Diseases: 24. Congenital Disorders of Glycosylation and Epilepsy, Susan Sparks; 25. Lysosomal Storage Diseases and Epilepsy, Pranoot Tanpaiboon; 26. Peroxisomal Diseases and Epilepsy, Gerald Raymond, Parastoo Jangouk, and Kristin W. Baranano; 27. Leukodystrophies and Epilepsy, Adeline Vanderver; IV. Conclusions: 28. Clinical Approach to Inherited Metabolic Epilepsies; Anna Pinto and Phillip L. Pearl