Neurology of Hereditary Metabolic Diseases of Children

General aspects of genetic metabolic diseases of the nervous system; the neurology of neonatal metabolic disease; early infantile progressive metabolic encephalopathies - clinical problems and diagnostic considerations; late-infantile progressive genetic encephalopathies; late-childhood progressive genetic encephalopathies; practical laboratory tests for the diagnosis of hereditary metabolic encephalopathies; distinctions between hereditary metabolic diseases and other diseases of the child's nervous system; special visual, auditory, crania, cutaneous and visceral abnormalities that aid in the diagnosis of hereditary metabolic encephalopathies; therapeutics and prophylaxis.