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Differential Diagnosis For Presentation/Progressive dementia Child Infant

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Presentation/Progressive dementia Child Infant
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Infectious Disorders (Specific Agent): Encephalitis, Dawsons/inclusion body; Progressive leukoencephalopathy/multifo
Metabolic, Storage Disorders: Metabolic disorders; Tay-Sachs disease; Cytochrome C Oxidase Deficiency/COX Complex Defect; French-Canadian type COX mitochondrial defect; HyperArgininemia; Ketotic hyperglycinemia, idiopathic; Methylmalonic acidemia/ketotic glycine; Propionicacidemia/ketotic glycinemia; Infantile mitochondrial myopathy/Cox defect; Hyperammonemia, hereditary; Sialidosis/Cherry Red Spot Myoclonus; Wilsons Disease; Ceroid lipofuschinosis/Late infantile (Jansky); Fructose intolerance, hereditary; Gangliosidosis, generalized (GM1); Gaucher's disease; Generalized gangliosidosis/GM2; Hartnup disease; Infantile ceroid lipofuscinosis/Finnish (Santvuori-Haltia); Juvenile ceroid lipofuscinosis/Batten-M; Juvenile GM2/Gangliosidosis type 3; Leukodystrophy/Arylsufatase deficiency; Niemann-Pick disease; Sandhoff disease; Sanfilippo's mucopolysaccharidosis synd; Tetrahydrobiopterin deficiency/Atypical PKU; Urea cycle/metabolic disorder
Congenital, Developmental Disorders: Alexander disease; Encephalopathy, myoclonic, infantile (Kinsbourne); Rett's syndrome; Landau-Kleffner Syndrome
Hereditary, Familial, Genetic Disorders: Infantile neuroaxonal dystrophy; Leukodytrophy, inherited/genetic; Schilder disease/Adrenoleukodystrophy; MELAS Encephalopathy; Dominant SCA/Spinal Cerebellar ataxias; Alpers cerebral degeneration of infancy; Canavan disease; Dentatorubral-Pallidoluysian Atrophy (DRPLA); Encephalomyelopathy/necro/subact/Leigh; Hereditary mitochondrial disorder; Hereditary/neurologic degeneration synd; Hermann's syndrome; Leukodystrophy, Krabbe; Menkes steely hair disease; Pelizaeus-Merzbacher disease; Refsum's disease
Usage, Degenerative, Necrosis, Age Related Disorders: Metachromatic leukodystrophy
Vegetative, Autonomic, Endocrine Disorders: Seizures
Poisoning (Specific Agent): Lead poisoning in children; Mercury/organic/methyl (Minamata) pois.; Lead encephalopathy
Synonyms: 0-11 years old, Child, Child (person), Child Youth, Childhood age person, Childhood age person (person), Children, Children (0-21), Dementia NEC, Presentation, Progressive
External Links Related to Presentation/Progressive dementia Child Infant: Google; Wikipedia; Merck; Images; PubMed (National Library of Medicine); NGC (National Guideline Clearinghouse); Medscape (eMedicine); Harrison's Online (accessmedicine); NEJM (The New England Journal of Medicine)

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