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Differential Diagnosis For Short stature Child: Metabolic, Storage Disorders

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List of current finding(s):

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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