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      The expanding spectrum of disorders with elevated plasma chitotriosidase activity: an update.

      Journal of Inherited Metabolic Disease
      Alagille Syndrome, blood, Fucosidosis, Galactose, Glycogen Storage Disease Type IV, Hexosaminidases, Humans, Hydrops Fetalis, Macrophages, metabolism

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          Abstract

          A striking elevation of plasma chitotriosidase activity, greater than 150 times the normal median value, was found in two galactosialidosis patients. Furthermore, increased plasma chitotriosidase activity, 10-53 times the normal median value, was also observed in fucosidosis, glycogen storage disease type IV, Alagille syndrome and hydrops fetalis due to congenital herpes virus infection.

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