Skip navigation

Refine by Type

Results 1 - 8 of 8 for Arginase deficiency
Did you mean arginine deficiency?
  1. Genetics Home Reference: Arginase deficiency From the National Institutes of Health (National Library of Medicine)  
    ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Arginase deficiency On this page: Description Genetic changes Inheritance Diagnosis ...
  2. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... Deficiency (Citrullinemia II) Argininosuccinate Lyase Deficiency (Argininosuccinic Aciduria) Arginase Deficiency ( Hyperargininemia) Ornithine Translocase Deficiency (HHH) Syndrome [ go to ...
  3. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
  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. 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 ...
  6. Urea Cycle Disease Overview From the National Institutes of Health (Rare Diseases Clinical Research Network)  
    ... be reduced in all urea cycle disorders, except arginase deficiency, in which it is elevated. A definitive diagnosis of CPSI deficiency, OTC deficiency, or NAGS deficiency is determined using the following: ... (arginase) Treatment Schedule: reducing the amount of ammonia in ...
  7. National Urea Cycle Disorders Foundation (National Urea Cycle Disorders Foundation)  
    ... in most states for ASA lyase, citrullinemia and arginase deficiency, making it possible to identify and treat affected ...
  8. ... in the body. These diseases include: Argininosuccinic aciduria Arginase deficiency Carbamyl phosphate synthetase (CPS) deficiency Citrullinemia N-acetyl ...