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Primary Hyperoxaluria
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Category Description:
This category contains information about Primary Hyperoxaluria. A rare inherited disorder, in which an enzyme deficiency causes overproduction of oxalate (aka oxalic acid) in the Liver, leading to the formation of stones in the Urinary Tract.
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See Also:
Health: Conditions and Illness: Genetic Disorders
Health: Conditions and Illness: Digestive Disorders: Liver
Health: Conditions and Illness: Rare Disorders
Health: Conditions and Illness: Genitourinary Disorders: Kidney: Stones
Genetics Home Reference: Primary Hyperoxaluria
- Describes this condition, types, prevalence, method of inheritance, management, and additional resources.
Mayo Clinic: Hyperoxaluria Center
- Resource for diagnosis, patient care, and research. Includes patient stories, treatment, and staff.
NORD: Hyperoxaluria, Primary (Type I)
- Gives synonyms, condition description, and related organizations.
What is Hyperoxaluria and Oxalosis?
- Discusses the disease process, causes, frequency, types, and milder forms.
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