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Differential Diagnosis For Short stature Child: Metabolic, Storage Disorders

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Short stature Child
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Metabolic, Storage Disorders: next: Deficiency Causes: Diabetes mellitus, poorly controlled; Neonatal hyperbilirubinemia; Renal tubular disorders/metabolic; Diabetes mellitus/juvenile (Type I); Mucopolysaccharidoses; Hurler's mucopolysaccharidosis syndrome; Renal tubular acidosis type IV; Tay-Sachs disease; Methylmalonic acidemia/ketotic glycine; Aminoacid enzyme/metabolic disorder; Orotic aciduria, hereditary; Wilsons Disease; Aminoaciduria; Beta-glucuronidase deficiency syndrome (MPS VII); Dyggve-Melchoir-Clausen dysplasia; Fucosidosis (Anderson-Fabry); Gangliosidosis, generalized (GM1); Gaucher's disease; Hartnup disease; Histiocytosis X; Hunter's mucopolysaccharidosis syndrome; Hurler-Scheie compound syndrome/mucopol; Lesch-Nyhan syndrome; Mannosidosis; Maple syrup urine disease; Morquio's mucopolysaccharidosis synd.; Niemann-Pick disease; Pseudo-Hurler polydystrophy (mucol'd 3); Tryptophanemia; Von Gierke's disease/glycogenosis I; Barth Syndrome/3 MethylGlutoconic aciduria/MGA II; Goldberg Syndrome

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