5 top medical experts on Familial Juvenile 2 Hyperuricemic Nephropathy across 0 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Familial Juvenile 2 Hyperuricemic Nephropathy: Familial juvenile hyperuricemic nephropathy type 2 is a rare autosomal dominantly inherited disease of childhood characterized by hypoproliferative anemia, hyperuricemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system (RAS).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: And Progressive Kidney Failure Anemia Early-Onset Hyperuricemia,  Familial Juvenile Hyperuricemic Nephropathy 2,  Hnfj2,  Ren-Related Kidney Disease


  

        

                    


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