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Diseases Gaucher’s disease

Storage disorders Glycogen storage diseases Gaucher s disease Wolman s disease... [Pg.64]

Wilson s disease, haemochromatosis, galactosaemia, glycogenosis type IV, ai-antitrypsin deficiency, tyrosin-aemia, idiopathic neonatal hepatitis, Niemann-Pick disease, Gaucher s disease, fructose intolerance, defective urea cycle, etc. [Pg.231]

Cystine storage disease Gaucher s disease Glycogen stora ge disease Juvenile, Tay-Sachs disease Niemann-Pick disease Tay-Sachs disease Chronic renal failure Hemolytic-uremic syndrome Nephrotic syndrome Benign recurrent intrahepatic cholestasis... [Pg.928]

Metabolic defects cause disturbances in the metabolism of sphingo-lipids in some diseases (for example, sphingolipidoses, infantile amaurotic idiocy, Tay-Sachs disease, Gaucher s disease, and meta-chromatic leucodystrophy). Klenk reported210 the anomalous accumulation of some gangliosides. [Pg.428]

Infantile Amaurotic Familial Idiocy (Tay-Sachs Disease) Gaucher s Disease Niemann-Pick Disease Leukodystrophies and Fabry s Disease... [Pg.143]

In contrast to what is observed in Tay-Sachs and in Neimann-Pick diseases, Gaucher s disease is not restricted to young children, but develops also in adults and even in old people. The first symptoms of the disease have been reported to occur in patients of 70 years however, at least one-third of Gaucher s disease cases are infants or young children. [Pg.191]

Gaucher s disease P-Giucosidase Cer-i-Gic Giucosyiceramide Enlarged liver and spleen, erosion of long bones, mental retardation in infants. [Pg.203]

An elevated activity of serum acid 3-glycerophosphatase was not specific for carcinoma, as Marshall and Amdor found it in 8% of patients with uncomplicated prostatic hyperplasia, in some patients with bone fractures, carcinoma involving the liver, and other diseases of bone and liver. This activity has also been reported to be elevated in 3 of 12 patients with Gaucher s disease. [Pg.216]

Lysosomotropic after intravenous injection to treat enzyme deficiencies (e.g., adult Gaucher s disease) Enzymes... [Pg.551]

Thrombolytic agent Thrombolytic agent Anticoagulant Haemophilia B Anti-cancer agent Cystic fibrosis Gaucher s disease Fabry disease Hyperuricaemia Mucopolysaccharidosis Oxygen toxicity Pompe disease... [Pg.356]

Gaucher s disease type I Fabry s disease Hurler s disease Pompe s disease Hurler s syndrome... [Pg.692]

Barton, N. W., Brady, R. O., Dambrosia, J. M. et al. Replacement therapy for inherited enzyme deficiency-macrophage-targeted glucocerebrosidase for Gaucher s disease. N. Engl. J. Med. 324 1464-1470,1991. [Pg.694]

Enzyme replacement Gaucher s disease, Fabry disease, and mucopolysaccharidosis Cerezyme, Fabrazyme, Aldurazyme... [Pg.96]

See other pages where Diseases Gaucher’s disease is mentioned: [Pg.187]    [Pg.912]    [Pg.181]    [Pg.533]    [Pg.618]    [Pg.1695]    [Pg.570]    [Pg.655]    [Pg.741]    [Pg.912]    [Pg.290]    [Pg.191]    [Pg.625]    [Pg.435]    [Pg.242]    [Pg.307]    [Pg.311]    [Pg.311]    [Pg.197]    [Pg.203]    [Pg.92]    [Pg.204]    [Pg.555]    [Pg.563]    [Pg.580]    [Pg.472]    [Pg.590]    [Pg.592]    [Pg.617]    [Pg.359]    [Pg.359]    [Pg.360]    [Pg.360]    [Pg.420]    [Pg.439]    [Pg.44]    [Pg.636]    [Pg.685]    [Pg.686]    [Pg.686]    [Pg.693]    [Pg.411]    [Pg.591]    [Pg.594]    [Pg.619]    [Pg.40]    [Pg.43]    [Pg.46]    [Pg.46]    [Pg.65]    [Pg.71]    [Pg.79]   
See also in sourсe #XX -- [ Pg.191 ]



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