Disease Information for Hyperoxaluria, primary

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Clinical Manifestations
Typical Clinical Presentation
Presentation/Recurrence same disease/renal transplant
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Past History
Past history/Kidney stone
Population Group
Child
Population/Pediatrics population
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Laboratory Tests
Abnormal Lab Findings - Increased
URINE Oxalate
URINE Oxalic acid crystals
Diagnostic Test Results
CT Scan
CT/Dexa-Scan Bone density Abnormal
X-RAY
Xray/Joint abnormal
Xray/Joint cartilage calcification
Xray/Rugger Jersey/Vertebral endplate dense bands/Spine
Xray/Sclerotic metaphyseal bands/Skeletal
Xray/Skeletal findings
Xray/Spine Abnormal
Xray/Spine bone-within-bone findings
Xray/KUB Cortico-Medullary junction multiple stones
Associated Diseases & Rule outs
Associated Disease & Complications
Ischemia, cardiac
Kidney stone/Nephrolithiasis/Urolithiasis
Male osteoporosis syndrome
Nephrocalcinosis
Osteoporosis/osteopenia
Pathologic fractures
Ureterolithiasis/stone in ureter
Metabolic Bone Disease
Calcium Containing Kidney Stones
Disease Mechanism & Classification
Class
CLASS/Primary organ/system disorder (ex)
CLASS/Renal/kidney involvement/disorder (ex)
CLASS/Urologic (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Osteoporosis Secondary
Pathophysiology/Calcium containing kidney stone process
Pathophysiology/Hereditary disease renal effect
Pathophysiology/Renal manifestations/involvement
Pathophysiology/Secondary Renal Failure
Process
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Metabolic/storage disorder (category)
Definition

Either of two genetic disorders characterized by urinary excretion of large amounts of oxalate, with nephrolithiasis, nephrocalcinosis, early onset of renal failure, and often a generalized deposit of calcium oxalate, resulting from a defect in glyoxalate metabolism.

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PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)
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