Condition
Hyperoxaluria, Primary
Urology / Fertility
Overview
A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Hyperoxaluria, Primary
- Topic type
- Condition
- Category
- Urology / Fertility
- MeSH classification
- C12.050.351.968.419.313.500|C12.200.777.419.313.500|C12.950.419.313.500|C16.320.565.202.460|C18.452.648.202.460
Preparing for an appointment about Hyperoxaluria, Primary
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- Write down your symptoms and when they started.
- Bring details of any medicines, supplements or previous treatments.
- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.