Section I. Introduction1. Neuroanatomy & Neuropathology of White Matter Disorders2. Cell biology of myelin3. Approaches to diagnosis in WMD4. MRI pattern recognition in white matter disease
Section II. Inherited Disorders5. Mitochondrial Disorders 6. Vanishing White Matter Disease7. Disorders with calcification in childhood8. Disorders with calcification or brain iron accumulation in adulthood9. Adrenoleukodystrophy10. Other peroxisomal disorders 11. Lysosomal storage disorders 12. Amino Acidopathies and Organic Acid Disorders 13. Hypomyelination (Myelin Disorders)14. Rare forms of hypomyelination and delayed myelination15. Chromosomal disorders 16. Very rare orphan disorders of childhood17. tRNA synthetases 18. Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia 19. Monogenic small vessel disease20. Amyloid related disorders 21. Disorders with prominent posterior fossa involvement
Section III. Treatments22. General approach to treatment of genetic leukoencephalopathies in children and adults23. Haematopoetic stem cell transplant 24. Gene therapy