Section I. General Considerations 1. Introduction 2. Molecular genetic mechanisms of neurodevelopmental and neurodegenerative disease 3. Techniques for genetic diagnosis: a practical guide 4. Genetic counseling and related issues 5. A Complimentary Approach: Metabolomics 6. Psychiatric disorders
Section II. Early-onset Presentations 7. Infant with Hypotonia 8. Neurodevelopmental Disorders 9. Metabolomic decompensation in an infant or young child 10. Neurocutaneous defects
Section III. Later-onset presentations 11. Metabolic decompensation in an adult 12. Stroke 13. Dementia and cognitive decline 14. Muscle weakness (Dystrophies) 15. Episodic flaccid muscle weakness (periodic paralysis)
Section IV. Movement Disorders 16. Ataxia and Spasticity 17. Involuntary movements and postures (Dystonia)
Section V. Neuropathy and Sensory Problems 18. Sensorimotor problem (peripheral neuropathy) 19. Visual loss 20. Hearing loss
Section VI. Paroxysmal Disorders 21. Epilepsy 22. Migraine