This book is the only up-to-date, comprehensive text on leukodystrophies. Its purpose is to summarize for the reader all aspects of the inherited disorders of myelin in children and adults. After a comprehensive overview of myelin and the role of oligodendrocytes, astrocytes and microglia in white matter disease, chapters are then devoted to individual disorders, covering their biochemical and molecular basis, genetics, pathophysiology, clinical features, diagnosis, treatment and screening. The final chapters address therapeutic approaches in leukodystrophies and present a clinical approach to diagnosing leukoencephalopathies in children and adults.
The book was conceived by Hugo Moser, whose research led to major developments in the treatment of adrenoleukodystrophy, and is dedicated to him by his colleagues.
Readership: Paediatric and adult neurologists, paediatricians, geneticists.
DEDICATION AND ACKNOWLEDGMENT x
FOREWORD xiAnn Moser
1 LEUKODYSTROPHY AND MYELIN 1Hugo Moser and Gerald V. Raymond
2 MYELINATION IN HEALTH AND DISEASE 5Grahame Kidd and Bruce D. Trapp
3 THE ROLE OF ASTROCYTES IN WHITE MATTER DISEASE 37Jörg Dietrich and Chris Pröschel
4 MICROGLIA AND LEUKODYSTROPHIES 60Patricia Musolino and Florian Eichler
5 X–LINKED ADRENOLEUKODYSTROPHY 75Gerald V. Raymond
6 KRABBE DISEASE (GLOBOID CELL LEUKODYSTROPHY) 90David A. Wenger
7 ALEXANDER DISEASE 106Daniel Flint and Michael Brenner
8 METACHROMATIC LEUKODYSTROPHY 130Volkmar Gieselmann and Ingeborg Krägeloh–Mann
9 CANAVAN DISEASE 156Kimberlee Michals and Reuben Matalon
10 PELIZAEUS MERZBACHER DISEASE: GENETIC MODELS AND MECHANISMS 170Klaus–Armin Nave and Ajit Singh Dhaunchak
11 THERAPEUTIC APPROACHES IN LEUKODYSTROPHIES 188Ali Fatemi and Charles Peters
12 CLINICAL APPROACH TO IDENTIFICATION OF LEUKOENCEPHALOPATHIES 209Sakkubai Naidu, Genila Bibat and Doris Lin
Florian Eichler is Director of the Leukodystrophy Service at Massachusetts General Hospital and Assistant Professor of Neurology at Harvard Medical School. His research focus is on the genetics of peroxisomal disorders, lipid metabolism, and spatial aspects of nuclear magnetic resonance spectroscopy.
Ali Fatemi is a pediatric neurologist in the Division of Neurology and Developmental Medicine and an investigator at the Hugo W. Moser Research Institute at Kennedy Krieger. He is also Assistant Professor of Neurology and Pediatrics at Johns Hopkins University. His research interest is in genetic and acquired conditions that affect the brain s white matter in newborns and infants.
Sakkubai Naidu is a research scientist at the Kennedy Krieger Institute and a Professor in the Departments of Neurology and Pediatrics at the Johns Hopkins University School of Medicine. She has a special interest in developmental and neurogenetic disorders affecting children and adults.