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Results 1 - 10 of 10 for Citrullinemia type I
  1. Citrullinemia is an inherited disorder that causes ammonia and other toxic substances to accumulate in the blood. Two types of citrullinemia have been described; they ...
  2. ... At least 118 mutations that cause type I citrullinemia have been identified in the ASS1 gene. Type I citrullinemia is a serious condition that usually appears in ...
  3. ... identified in people with adult-onset type II citrullinemia. This condition causes neurological problems, such as confusion, ... problems in people with adult-onset type II citrullinemia.Mutations in the SLC25A13 gene also have been ...
  4. What Is a Urea Cycle Disorder? (National Urea Cycle Disorders Foundation)  
    Metabolic Disorders/Specifics ... Metabolic Disorders ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... National Urea Cycle Disorders Foundation
  5. 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. ...
  6. 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 ...
  7. 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 ...
  8. ... aciduria Arginase deficiency Carbamyl phosphate synthetase (CPS) deficiency Citrullinemia N-acetylglutamate synthetase (NAGS) deficiency Ornithine transcarbamylase (OTC) ...
  9. Newborn Screening Tests for Your Baby (March of Dimes Foundation)  
    Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation
  10. ... depression, episodes of mania, and other abnormal moods); citrullinemia (condition that causes build-up of ammonia in ...