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Differential Diagnosis For Hepatosplenomegaly: Metabolic, Storage Disorders

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Hepatosplenomegaly
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Metabolic, Storage Disorders: next: Congenital Causes: Hypertriglyceridemia; Lipodystrophy/diabetes, lipoatrophic; Amyloidosis, hepatosplenic; Amyloidosis, secondary; Chylomicronemia syndrome; Hemochromatosis; Hurler's mucopolysaccharidosis syndrome; Cerebral Gaucher's of infants (acute); Wolman Disease; Aspartylglycosaminuria; Beta-glucuronidase deficiency syndrome (MPS VII); Cholesteryl ester storage disease; DiFerrente syndrome (Mucopolysaccharidosis VIII); Fucosidosis (Anderson-Fabry); Gangliosidosis, generalized (GM1); Gaucher's disease; Glycogen storage diseases; Histiocytosis X; Morquio's mucopolysaccharidosis synd.; Niemann-Pick disease; Sandhoff disease; Sanfilippo's mucopolysaccharidosis synd; Storage (storage-cell) disorders; Tangier's disease; Von Gierke's disease/glycogenosis I; Goldberg Syndrome

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