What is hyperoxaluria?
hyperoxaluria is a chronic health in which a person has an unusually high concentration of salt called oxalate in urine. Excess oxalate tends to build in the kidneys and can lead to the formation of kidney stones. Hyperoxaluria may be inherited genetic disorder or the outcome of the diet too rich in oxalate. An individual who has symptoms, including reduced urine production, nausea and fatigue, should see a doctor as soon as possible to test for hyperoxaluria and avoid dangerous complications.
Normally, oxalate is found in food, liver processed and excreted like kidney waste. A person with hyperoxaluria is not able to correctly decompose oxalate, leading to excessive amount of salt in the kidneys and urinary tract. Excess oxalate then binds with calcium to create insoluble crystals called kidney stones. Once stones begin to develop, the individual is likely to experience painful, occasional urination, frequent episodes of nausea and vomiting and general feeling of fatigue and weakness. Without treatment, kidney stones can cause severe blockage and lead to abdominal pain, kidney inflammation and possible kidney failure.
Most cases of hyperoxaluria are the result of specific genetic mutations that inhibit the production of certain liver enzymes, making the liver unable to break down the oxalate. This condition can also occur if there is too much oxalate in a person's diet. Foods such as chocolate, nuts and leaf green contain high oxalate levels and too many such foods can overwhelm liver and kidney. In addition, gastrointestinal disorders can occasionally prevent the oxalate from being properly distributed and excluded.
A person who believes that he may suffer from Hyperoxaluria and learn about treatment options. The doctor can analyze urine and blood samples to check abnormal levels of salts and minerals. In addition, it can perform ultrasound or computer tomographic withKenovní to look for signs of kidney stones. The patient may be dependent on a kidney specialist to perform further tests and confirm the diagnosis.
Treatment of hyperoxaluria depends on basic causes. Dietary conditions are usually the easiest to treat and patients are instructed to avoid food -rich foods and drink cranberry juice and water to clean the kidneys. Patients with genetic hyperoxaluria are usually prescribed drugs to help control body oxalate levels. If the condition has ceded so much that it is likely that renal failure, it may be necessary to undergo kidney and liver transplantation to avoid life -threatening problems. Most people are able to experience full enforcement after proper handling and watch their documentors' commands.