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HP2

Introduction: HP2

Description of HP2

HP2 (medical condition): A rare inherited inborn metabolic disorder characterized by...more »

See also:

Primary hyperoxaluria type 2:
  »Introduction: Primary hyperoxaluria type 2
  »Symptoms of Primary hyperoxaluria type 2
  »Treatments for Primary hyperoxaluria type 2

HP2: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

HP2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that HP2, or a subtype of HP2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

HP2 as a Disease

HP2: Another name for Primary hyperoxaluria type 2 (or close medical condition association).
  »Introduction: Primary hyperoxaluria type 2
  »Symptoms of Primary hyperoxaluria type 2
  »Treatments for Primary hyperoxaluria type 2

HP2: Related Diseases

HP2: HP2 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of HP2 (Primary hyperoxaluria type 2)

Some of the symptoms of HP2 incude:

Treatments for HP2 (Primary hyperoxaluria type 2)

Treatments for HP2 (Primary hyperoxaluria type 2) include:

  • Pyridoxine (Vitamin B6) can reduce levels of oxalate made by the liver - this therapy works better for some people than others.
  • Neutral phosphates, citrates and magnesium may also help with reducing the formation of urinary stones
  • Intake of oxalate in the diet should also be minimized though this doesn't seem to have a huge impact on the disease
  • Increase fluid intake
  • Lithotripsy to remove urinary stones

Treatment of HP2: For more treatment information about HP2, see treatment of Primary hyperoxaluria type 2 (HP2)

Terms associated with HP2:

Terms Similar to HP2:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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