Healthcare utilization, quality of life, and work productivity associated with primary hyperoxaluria: a cross-sectional web-based us survey

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• who: David S. Goldfarb from the Primary hyperoxaluria (PH) is a family of three ultra-rare, autosomal recessive, metabolic disorders leading to markedly elevated levels of endogenous oxalate in plasma and urine, which is associated with frequent kidney stones, chronic kidney disease and kidney failure, and serious complications due to systemic oxalosis [1-9]The distinct genetic disorders (PH1, PH2, PH3) together have an estimated prevalence of , per, in the United States have published the Article: Healthcare utilization, quality of life, and work productivity associated with primary hyperoxaluria: a cross-sectional web-based US survey, in the . . .
  

   

  

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