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Mild Metabolic Hyperoxaluria. A New Syndrome

  • G. A. Rose
Part of the The Bloomsbury Series in Clinical Science book series (BLOOMSBURY)

Abstract

The term “mild metabolic hyperoxaluria” (MMH) is being used to define a group of patients with the following characteristics:
  1. 1.

    The patients all have hyperoxaluria compared to healthy individuals of the same age and sex. Usually the urinary oxalate is only slightly elevated although in one or two cases very high levels have been seen

     
  2. 2.

    The word “metabolic” signifies that urinary glycollate is also elevated, approximately matching the urinary excretion of oxalate. This raised urinary glycollate proves that the hyperoxaluria is not due to over-ingestion or over-absorption of dietary oxalate (Rose and Kasidas 1979)

     
  3. 3.

    The clinical course is of severe and recurrent urolithiasis with stones made of pure calcium oxalate

     
  4. 4.

    In some cases it has been possible to measure oxalate in plasma and urine samples taken simultaneously and to show that both levels are raised. Hence the hyperoxaluria is due to raised plasma level and not to primary renal loss of oxalate. Plasma glycollate has not been measured, but it seems likely that it too is raised

     
  5. 5.

    Some patients respond dramatically to only 10 mg per day of pyridoxine. Others require higher doses and yet others will not respond even to 800 mg per day. This and other factors are described below

     

Keywords

Primary Hyperparathyroidism Parathyroid Adenoma Calcium Oxalate Renal Tubular Acidosis Urinary Oxalate 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

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Copyright information

© Springer-Verlag Berlin Heidelberg 1988

Authors and Affiliations

  • G. A. Rose

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