201 top medical experts on Argininosuccinic Aciduria across 28 countries and 10 U.S. states, including 32 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Argininosuccinic Aciduria: Rare autosomal recessive disorder of the urea cycle which leads to the accumulation of argininosuccinic acid in body fluids and severe hyperammonemia. Clinical features of the neonatal onset of the disorder include poor feeding, vomiting, lethargy, seizures, tachypnea, coma, and death. Later onset results in milder set of clinical features including vomiting, failure to thrive, irritability, behavioral problems, or psychomotor retardation. Mutations in the argininosuccinate lyase gene cause the disorder.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Urea Cycle Disorders (1,187).
  4. Clinical Trials ClinicalTrials.gov : at least 6 including 2 Completed, 3 Recruiting
  5. Synonyms: Arginino Succinase Deficiency


  

        

                    


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