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Results 1 - 6 of 6 for Argininosuccinate lyase deficiency
  1. Genetics Home Reference: Argininosuccinic aciduria From the National Institutes of Health (National Library of Medicine)  
    ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Argininosuccinic aciduria On this page: Description Genetic changes Inheritance Diagnosis ...
  2. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... Synthetase Deficiency (Citrullinemia I) Citrin Deficiency (Citrullinemia II) Argininosuccinate Lyase Deficiency (Argininosuccinic Aciduria) Arginase Deficiency ( Hyperargininemia) Ornithine Translocase Deficiency ( ...
  3. ... down ammonia in the body. These diseases include: Argininosuccinic aciduria Arginase deficiency Carbamyl phosphate synthetase (CPS) deficiency Citrullinemia ...
  4. Metabolic Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
  5. National Urea Cycle Disorders Foundation (National Urea Cycle Disorders Foundation)  
    ... for Transformative Research. UPDATE ON ARGININE THERAPY FOR ARGININOSUCCINIC ACIDURIA AND ITS EFFECTS ON LIVER DYSFUNCTION: Urea Cycle ...
  6. Newborn Screening (National Library of Medicine)  
    Your newborn infant has screening tests before leaving the hospital. There may be different tests depending on the state where you live. They include Tests ...