[Neuroaxonal dystrophy, infantile]. 2001

T Kondoh, and T Matsumoto
Department of Pediatrics, Nagasaki University School of Medicine.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D019150 Neuroaxonal Dystrophies A nonspecific term referring both to the pathologic finding of swelling of distal portions of axons in the brain and to disorders which feature this finding. Neuroaxonal dystrophy is seen in various genetic diseases, vitamin deficiencies, and aging. Infantile neuroaxonal dystrophy is an autosomal recessive disease characterized by arrested psychomotor development at 6 months to 2 years of age, ataxia, brain stem dysfunction, and quadriparesis. Juvenile and adult forms also occur. Pathologic findings include brain atrophy and widespread accumulation of axonal spheroids throughout the neuroaxis, peripheral nerves, and dental pulp. (From Davis & Robertson, Textbook of Neuropathology, 2nd ed, p927) Neuroaxonal Dystrophy, Juvenile,Seitelberger's Disease,Adult Neuroaxonal Dystrophy,Infantile Neuroaxonal Dystrophy,Juvenile Neuroaxonal Dystrophy,Late Infantile Neuroaxonal Dystrophy,NBIA, PLA2G6-Related,NBIA2A,Neuroaxonal Dystrophy, Adult,Neuroaxonal Dystrophy, Infantile,Neuroaxonal Dystrophy, Late Infantile,Neurodegeneration With Brain Iron Accumulation 2A,Neurodegeneration, PLA2G6-Associated,Seitelberger Disease,Disease, Seitelberger,Disease, Seitelberger's,Dystrophy, Adult Neuroaxonal,Dystrophy, Infantile Neuroaxonal,Dystrophy, Juvenile Neuroaxonal,Dystrophy, Neuroaxonal,NBIA, PLA2G6 Related,Neuroaxonal Dystrophy,Neurodegeneration, PLA2G6 Associated,PLA2G6-Associated Neurodegeneration,PLA2G6-Related NBIA,Seitelbergers Disease

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