What is primary hyperoxaluria?
Primary hyperoxaluria is a rare condition characterized by the overproduction of a substance called oxalate (also called oxalic acid).
primary hyperoxaluria: A rare metabolic disease caused by the liver making too much oxalic acid that is excreted in the urine of the affected person.
probe: Small device for measuring and testing.
primary hyperoxaluria - caused by mutations in the AGXT gene Researchers have identified about 50 AGXT mutations that cause type 1 primary hyperoxaluria.
Primary hyperoxaluria is an inherited disorder in which too much oxalate in the urine is the main problem.
Secondary hyperoxaluria results from specific conditions that cause high levels of urinary oxalate.
Primary hyperoxaluria type 1 ... gangrene
Protoporphyria ... thickened skin
Prurigo ... increased pigmentation, lichenification, thickened skin
Prurigo nodularis of Hyde ... increased pigmentation, lichenification, thickened skin ...
Vitamin B6, or pyridoxine, is used to treat people with primary hyperoxaluria, a severe inherited disorder. Patients should not try to self-medicate with vitamin B6.
Genetics Home Reference - Primary hyperoxaluria
Counsyl - Primary Hyperoxaluria Type 1
Oxalosis and Hyperoxaluria Foundation ...
Alport syndome
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vivax, Myosin III, Neuropathies, Shoulder-Girdle, Nitrospan, Organization, Physician-Hospital, Ornithine Transcarbamylase, Outcome Study, Ureteral Calculus, Urogranoic Acid, Variables, Intermediate, Variegate Porphyria, Primary Hyperoxalurias, ...
 See also: Hyperoxaluria, Kidney, Oxaluria, Kidney stones, Symptom
  
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