255 top medical experts on Primary hyperoxaluria type 1 across 31 countries and 14 U.S. states, including 99 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Primary hyperoxaluria type 1: Primary hyperoxaluria type 1 (PH1) is a rare disorder that mainly affects the kidneys. It results from buildup of a substance called oxalate, which normally is filtered through the kidneys and excreted in the urine. In people with PH1, the accumulated oxalate is deposited in the kidneys and urinary tract. It combines with calcium, forming the main component of kidney and bladder stones (calcium oxalate).
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Organizations Providing General Support

  • Synonyms: Alanine-glyoxylate aminotransferase deficiency,  Glycolic aciduria,  Hepatic AGT Deficiency,  Type I Primary Hyperoxaluria,  Oxalosis 1,  Oxalosis I,  Peroxisomal Alanine:Glyoxylate Aminotransferase Deficiency,  Peroxisomal alanine glyoxylate aminotransferase deficiency,  Serine:Pyruvate Aminotransferase Deficiency


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