301 top medical experts on congenital Nephrosis across 48 countries and 16 U.S. states, including 122 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. congenital Nephrosis: A rare primary glomerular group of diseases characterized by the triad of edema, massive, or nephrotic-range, proteinuria and hypoalbuminemia, for which there is no known cause. Depending on response to treatment, disease is distinguished into steroid-sensitive nephrotic syndrome (SSNS) and steroid-resistant nephrotic syndrome (SRNS), with the latter being further divided, depending on occurrence, into familial or sporadic forms.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Congenital nephrotic syndrome 1,  Finnish type Congenital nephrotic syndrome,  Finnish congenital nephrosis,  Finnish type congenital Nephrosis 1,  Type 3 Early-Onset Nephrotic Syndrome,  Idiopathic Nephrotic Syndrome,  Type 1 Nephrotic Syndrome,  Type 2 Nephrotic Syndrome,  Type 3 Nephrotic Syndrome,  Nphs3


  

        

                    


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