225 top medical experts on Citrullinemia across 26 countries and 10 U.S. states, including 54 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Citrullinemia: A group of diseases related to a deficiency of the enzyme argininosuccinate synthase which causes an elevation of serum levels of citrulline. In neonates, clinical manifestations include lethargy, hypotonia, and seizures. Milder forms also occur. Childhood and adult forms may present with recurrent episodes of intermittent weakness, lethargy, ataxia, behavioral changes, and dysarthria. (From Menkes, Textbook of Child Neurology, 5th ed, p49)
  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 7 including 2 Completed, 2 Recruiting
  5. Synonyms: ASS Deficiency,  Argininosuccinate Synthase Deficiency Disease,  Argininosuccinate Synthetase Deficiency,  Argininosuccinic Acid Synthetase Deficiency,  Citrullinemia 1,  Citrullinemia Type 1,  Classic Citrullinemia,  Argininosuccinate Synthase Deficiency Disease,  Argininosuccinic Acid Synthase Deficiency Disease


  

        

                    


    Computing Expert Listing ...

);