Hyperoxaluria

Hyperoxaluria
DiseasesDB	31642
eMedicine	med/3027

WikiDoc Resources for Hyperoxaluria
Articles
Most recent articles on Hyperoxaluria Most cited articles on Hyperoxaluria Review articles on Hyperoxaluria Articles on Hyperoxaluria in N Eng J Med, Lancet, BMJ
Media
Powerpoint slides on Hyperoxaluria Images of Hyperoxaluria Photos of Hyperoxaluria Podcasts & MP3s on Hyperoxaluria Videos on Hyperoxaluria
Evidence Based Medicine
Cochrane Collaboration on Hyperoxaluria Bandolier on Hyperoxaluria TRIP on Hyperoxaluria
Clinical Trials
Ongoing Trials on Hyperoxaluria at Clinical Trials.gov Trial results on Hyperoxaluria Clinical Trials on Hyperoxaluria at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on Hyperoxaluria NICE Guidance on Hyperoxaluria NHS PRODIGY Guidance FDA on Hyperoxaluria CDC on Hyperoxaluria
Books
Books on Hyperoxaluria
News
Hyperoxaluria in the news Be alerted to news on Hyperoxaluria News trends on Hyperoxaluria
Commentary
Blogs on Hyperoxaluria
Definitions
Definitions of Hyperoxaluria
Patient Resources / Community
Patient resources on Hyperoxaluria Discussion groups on Hyperoxaluria Patient Handouts on Hyperoxaluria Directions to Hospitals Treating Hyperoxaluria Risk calculators and risk factors for Hyperoxaluria
Healthcare Provider Resources
Symptoms of Hyperoxaluria Causes & Risk Factors for Hyperoxaluria Diagnostic studies for Hyperoxaluria Treatment of Hyperoxaluria
Continuing Medical Education (CME)
CME Programs on Hyperoxaluria
International
Hyperoxaluria en Espanol Hyperoxaluria en Francais
Business
Hyperoxaluria in the Marketplace Patents on Hyperoxaluria
Experimental / Informatics
List of terms related to Hyperoxaluria

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Hyperoxaluria is an excessive urinary excretion of oxalate. Individuals with hyperoxaluria often have calcium oxalate kidney stones.

Differential Diagnosis of Underlying Causes

Chemicals

• Ethylene glycol
• Oxalate poisoning
• Cellulose sodium phosphate

Genetic

Autosomal recessive conditions include:

• Hyperoxaluria, primary type 1

Synonyms include Oxalosis type 1; Oxalosis, primary type 1; Alanine-gloxylate aminotransferase (hepatic) deficiency; Glycolic aciduria

• Hyperoxaluria, primary type 2

Synonyms include Oxalosis type 2; D-glycerate dehydrogenase deficiency; Glycerate dehydrogenase deficiency; Hydroxypyruvate reductase / glyoxylate reductase deficiency

Idiopathic

Idiopathic hyperoxaluria

Nutritional conditions

• Malabsorption syndrome
• Enteric hyperoxaluria