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Possible Causes For Mental retardation - Causes: Metabolic, Storage Disorders

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Mental retardation - Causes
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Metabolic, Storage Disorders: next: Deficiency Causes: Mucopolysaccharidoses; Hurler's mucopolysaccharidosis syndrome; Hypobetalipoproteinemia; Kernicterus; Tay-Sachs disease; Abetalipoproteinemia (Bassen Kornzweig); Hydroxyprolinemia, congenital; Combined carboxylase/Biotinidase deficiency; HyperArgininemia; Ketotic hyperglycinemia, idiopathic; Methylmalonic acidemia/ketotic glycine; Phenylketonuria/PKU; Propionicacidemia/ketotic glycinemia; Pyruvate Dehydrogenase Complex Deficiency/PDCD; Adenyl succinate lysate deficiency; Phosphoglycerate Kinase Deficiency/Systemic homozygous PGKD; Alphamethylacetoacetate accumulation; Aminoacid enzyme/metabolic disorder; Beta-hydroxyisolvaleric acidemia; Cerebral lipidosis disorder; Crigler-Najjar syndrome; Hyperglycinemia, nonketotic; Lysinemia; Ornithine Transcarbamylase (OTC) defic.; Prolinemia/type II; Saccharopinuria/lysine metabolism defect; Sialidosis/Cherry Red Spot Myoclonus; Succinic Semialdehyde dehydrogenase Deficiency; Tyrosinemia, hereditary; Adult ceroid lipofuscinosis/Kufs; Alpha-NAGA deficency (Schindler); Aminoaciduria; Aspartylglycosaminuria; Beta-glucuronidase deficiency syndrome (MPS VII); Cystathioninuria; DiFerrente syndrome (Mucopolysaccharidosis VIII); Dyggve-Melchoir-Clausen dysplasia; Fucosidosis (Anderson-Fabry); Galactosemia; Gangliosidosis, generalized (GM1); Glutaric aciduria/Acidemia; Hartnup disease; Histidinemia; Homocystinuria/homocystinemia; Hunter's mucopolysaccharidosis syndrome; Juvenile ceroid lipofuscinosis/Batten-M; Lesch-Nyhan syndrome; Mannosidosis; Maple syrup urine disease; Morquio's mucopolysaccharidosis synd.; Mucolipidosis IV (Bermans Syndrome); Niemann-Pick disease; Pipecolic acidemia; Sanfilippo's mucopolysaccharidosis synd; Sarcosinemia; Tetrahydrobiopterin deficiency/Atypical PKU; Transcobalamin II deficiency; Tryptophanemia; Urea cycle/metabolic disorder; Goldberg Syndrome

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