Hereditary And Degenerative Disorders

Neuronal ceroid lipofuscinosis, especially NCL-2

Cerebrosidoses, especially type II

Leukodystrophies, especially Canavan's disease (neonatal form) and Krabbe's disease

Aminoacidopathies, especially maple syrup urine disease, urea cycle disorders, propionie acidemia, methylmalonie acidemia

Mitochondrial enzyme defects, especially Leigh's disease, Alpers disease MERFF, MELAS, fatty acid oxidation disorders

Conditions associated with generalized seizures, especially tuberous sclerosis and Sturge-Weber syndrome

Chapter

The degenerative dementias

Movement disorders

Ataxias

Degenerative motor, sensory, and autonomic disorders

Endogenous metabolic disorders

Exogenous acquired metabolic disorders of the nervous system: toxins and illicit drugs

Nutritional deficiencies and syndromes associated with alcoholism

Viral infections Nonviral infections

Transmissible spongiform encephalopathies

HIV and AIDS

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