allopurinol and Chorea

allopurinol has been researched along with Chorea* in 11 studies

Other Studies

11 other study(ies) available for allopurinol and Chorea

ArticleYear
Effect of allopurinol on pyrimidine metabolism in the Lesch-Nyhan syndrome.
    Lancet (London, England), 1970, Oct-17, Volume: 2, Issue:7677

    Topics: Allopurinol; Athetosis; Child; Chorea; Compulsive Behavior; Humans; Intellectual Disability; Orotic Acid; Purine-Pyrimidine Metabolism, Inborn Errors; Purines; Pyrimidines; Self Mutilation; Uric Acid

1970
Determination of urinary purines in hyperuricosuric children by thin-layer chromatography.
    The Journal of laboratory and clinical medicine, 1970, Volume: 76, Issue:1

    Topics: Allopurinol; Athetosis; Child; Child, Preschool; Chorea; Chromatography, Thin Layer; Densitometry; Humans; Hypoxanthines; Intellectual Disability; Male; Nucleosides; Purine-Pyrimidine Metabolism, Inborn Errors; Purines; Self Mutilation; Uric Acid; Xanthines

1970
Mechanism of excessive purine biosynthesis in hypoxanthine-guanine phosphoribosyltransferase deficiency.
    The Journal of clinical investigation, 1970, Volume: 49, Issue:5

    Certain gouty subjects with excessive de novo purine synthesis are deficient in hypoxanthineguanine phosphoribosyltransferase (HG-PRTase [EC 2.4.2.8]). The mechanism of accelerated uric acid formation in these patients was explored by measuring the incorporation of glycine-(14)C into various urinary purine bases of normal and enzyme-deficient subjects during treatment with the xanthine oxidase inhibitor, allopurinol. In the presence of normal HG-PRTase activity, allopurinol reduced purine biosynthesis as demonstrated by diminished excretion of total urinary purine or by reduction of glycine-(14)C incorporation into hypoxanthine, xanthine, and uric acid to less than one-half of control values. A boy with the Lesch-Nyhan syndrome was resistant to this effect of allopurinol while a patient with 12.5% of normal enzyme activity had an equivocal response. Three patients with normal HG-PRTase activity had a mean molar ratio of hypoxanthine to xanthine in the urine of 0.28, whereas two subjects who were deficient in HG-PRTase had reversal of this ratio (1.01 and 1.04). The patterns of (14)C-labeling observed in HG-PRTase deficiency reflected the role of hypoxanthine as precursor of xanthine. The data indicate that excessive uric acid in HG-PRTase deficiency is derived from hypoxanthine which is insufficiently reutilized and, as a consequence thereof, catabolized inordinately to uric acid. The data provide evidence for cyclic interconversion of adenine and hypoxanthine derivatives. Cleavage of inosinic acid to hypoxanthine via inosine does not contribute significantly to the formation of uric acid in either normal man or in patients with HG-PRTase deficiency.HG-PRTase was not completely absent in red blood cells from a boy with the Lesch-Nyhan syndrome; with hypoxanthine as substrate, the activity in erythrocyte hemolysates was 0.64% of normal values.

    Topics: Adult; Allopurinol; Athetosis; Carbon Isotopes; Child; Chorea; Compulsive Behavior; Deficiency Diseases; Glycine; Gout; Guanine; Humans; Hypoxanthines; Inositol; Intellectual Disability; Metabolism, Inborn Errors; Nucleosides; Purines; Self Mutilation; Transferases; Uric Acid

1970
The influence of adenine on the clinical features and purine metabolism in the Lesch-Nyhan syndrome.
    Acta paediatrica Scandinavica, 1970, Volume: 59, Issue:3

    Topics: Adenine; Allopurinol; Athetosis; Bone Marrow; Carbon Isotopes; Child; Child, Preschool; Chorea; Compulsive Behavior; Diet Therapy; Erythrocytes; Folic Acid; Glycine; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Movement Disorders; Purines; Self Mutilation; Transferases; Uric Acid; Vitamin B 12

1970
The significance of the deficiency state in Lesch-Nyhan disease.
    Acta paediatrica Scandinavica, 1970, Volume: 59, Issue:3

    Topics: Allopurinol; Amino Acids; Athetosis; Carbon Isotopes; Child, Preschool; Chorea; Compulsive Behavior; Diet Therapy; Glutamates; Glycine; Humans; Infant; Intellectual Disability; Male; Metabolism, Inborn Errors; Movement Disorders; Purines; Self Mutilation; Uric Acid

1970
Preliminary results from high-resolution analyses of ultraviolet-absorbing and carbohydrate constituents in several pathologic body fluids.
    Clinical chemistry, 1970, Volume: 16, Issue:8

    Topics: Adolescent; Adult; Alkaptonuria; Allopurinol; Amniotic Fluid; Athetosis; Carbohydrates; Chorea; Chromatography, Ion Exchange; Compulsive Behavior; Female; Gout; Humans; Hypertension; Infant; Infant, Newborn; Intellectual Disability; Male; Maple Syrup Urine Disease; Methods; Middle Aged; Nephritis; Nicotinic Acids; Phenols; Pregnancy; Purine-Pyrimidine Metabolism, Inborn Errors; Purines; Self Mutilation; Spectrophotometry; Sulfuric Acids; Ultraviolet Rays; Uric Acid; Xanthines

1970
Lesch-Nyhan syndrome.
    Paediatria Universitatis Tokyo, 1970, Volume: 18

    Topics: Allopurinol; Athetosis; Benzofurans; Brain; Child; Child, Preschool; Chorea; Compulsive Behavior; Erythrocytes; Female; Guanine; Humans; Hypoxanthines; Infant; Intellectual Disability; Japan; Kidney; Lesch-Nyhan Syndrome; Liver; Male; Proteinuria; Purine-Pyrimidine Metabolism, Inborn Errors; Self Mutilation; Transferases; Uric Acid

1970
[Juvenile hyperuricemia, gout and cerebral palsy (Lesch-Nyhan syndrome)].
    Zeitschrift fur Kinderheilkunde, 1969, Oct-09, Volume: 107, Issue:1

    Topics: Adolescent; Allopurinol; Athetosis; Cerebral Palsy; Chorea; Gout; Humans; Male; Uric Acid

1969
Hyperuricemia and mental retardation with athetosis and self-mutilation.
    American journal of diseases of children (1960), 1967, Volume: 113, Issue:2

    Topics: Allopurinol; Athetosis; Body Height; Body Weight; Child; Child, Preschool; Chorea; Humans; Infant; Intellectual Disability; Male; Probenecid; Self Mutilation; Uric Acid; Xanthine Oxidase

1967
[Congenital hyperuricemia with neurologic, renal and blood disturbances].
    Archives francaises de pediatrie, 1967, Volume: 24, Issue:5

    Topics: Adolescent; Allopurinol; Anemia, Macrocytic; Athetosis; Chorea; Gout; Humans; Intellectual Disability; Male; Nephritis, Interstitial; Neurologic Manifestations; Uric Acid

1967
Inherited disorder of purine metabolism. Correlation between central nervous system dysfunction and biochemical defects.
    JAMA, 1967, Oct-16, Volume: 202, Issue:3

    Topics: Adolescent; Allopurinol; Aminohydrolases; Athetosis; Brain; Central Nervous System Diseases; Cerebral Palsy; Chorea; Erythrocytes; Fibroblasts; Glucosyltransferases; Humans; Hypoxanthines; Intellectual Disability; Liver; Male; Purine-Pyrimidine Metabolism, Inborn Errors; Purines; Self Mutilation; Spasm; Xanthines

1967