Phosphaturia, Phosphuria

Phosphaturia and Phosphuria are medical terms that describe a condition in which the level of phosphate in the urine is elevated, causing it to become cloudy. Both of these terms are used to refer to the same condition, but with different nuances.

Phosphates are minerals essential to human health found in food and nutrients. However, when the level of phosphate in the urine is elevated, it may indicate the presence of kidney or urinary system problems.

Phosphaturia is a condition in which the level of phosphate in the urine is increased due to increased urinary excretion. Most often this occurs due to kidney problems. Symptoms of phosphaturia may include cloudy urine, as well as the formation of stones (calculi) in the kidneys or bladder.

Phosphuria is also an increased excretion of phosphates in the urine, but in this case the cause of this condition may be associated with an increase in the intake of phosphates in the body. This can happen, for example, if you consume excess foods rich in phosphates, such as dairy products or carbonated drinks. Increased phosphate excretion may also be associated with thyroid dysfunction.

In any case, increased levels of phosphates in the urine are a symptom of disease and require consultation with a doctor. To diagnose phosphaturia or phosphuria, urine and blood tests, as well as ultrasound examination of the kidneys and bladder, may be prescribed. Treatment will depend on the cause of the elevated phosphate levels in the urine and may include dietary changes, medications, or surgery.

In conclusion, phosphaturia and phosphuria are conditions in which the level of phosphate in the urine is elevated, which may indicate the presence of kidney or urinary system disease. If you have symptoms of cloudy urine or other signs of kidney problems, see your doctor for diagnosis and treatment. Good health is the key to a long and happy life.



Phosphaturia can be defined as hereditary familial hypophosphaturic phosphate diabetes. It is also called hereditary hypokalemic urinary syndrome, hereditary phosphaturic osteodystrophy, or hereditary diaphyseal dysplasia. A test must be taken to detect increased levels of phosphate in the urine. Increased phosphates in the urine are observed during pregnancy. Also observed when taking antacids. If the level of calcium and ionized phosphorus in the blood is elevated, the patient will be diagnosed with secondary hyperparathyroidism.

Phosphorisuria indicates a disorder of calcium metabolism in bone tissue. Phosphorus can be excreted from the kidneys - then the process is called phosphaturia. Such patients are at risk of developing renal edema, cysts, and stones. The sooner the disease is detected in the mother after the birth of the child, the higher the likelihood of remission of hyperphosphaturia - the patient permanently loses or temporarily ceases to secrete the substance in large quantities. The anomaly is a marker of hereditary skeletal diseases, but does not affect the vital organs of the child. Therefore, treatment is not required until 2 years of his life. General restorative therapy is indicated for the normal course of the disease, and if the pathology is complicated by infections, hospitalization is necessary.