The Peroxisomal Disorders
Copyright policy )The Peroxisomal Disorders
It is now recognized that absence of normal peroxisomal function is associated with far-reaching and devastating consequences. A group of diverse genetic disorders in which either defective formation of the peroxisome or deficiency of one or more of its constituent enzymes is the central pathogenetic feature has recently been described. Three principal conditions are discussed.
- Albert Einstein College of Medicine United States
- Johns Hopkins University United States
Adult, Chromosome Aberrations, Fatty Acids, Infant, Newborn, Chromosome Disorders, Diffuse Cerebral Sclerosis of Schilder, Syndrome, Microbodies, Lipid Metabolism, Inborn Errors, Liver, Central Nervous System Diseases, Child, Preschool, Humans, Abnormalities, Multiple, Adrenoleukodystrophy, Child
Adult, Chromosome Aberrations, Fatty Acids, Infant, Newborn, Chromosome Disorders, Diffuse Cerebral Sclerosis of Schilder, Syndrome, Microbodies, Lipid Metabolism, Inborn Errors, Liver, Central Nervous System Diseases, Child, Preschool, Humans, Abnormalities, Multiple, Adrenoleukodystrophy, Child
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