Phosphaturia
Detailed article on Phosphaturia for medical students
Phosphaturia | |
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[[File:|250px|]] | |
Synonyms | N/A |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Excessive phosphate in urine |
Complications | Hypophosphatemia, Osteomalacia |
Onset | N/A |
Duration | N/A |
Types | N/A |
Causes | Renal tubular disorders, Hyperparathyroidism, Vitamin D deficiency |
Risks | N/A |
Diagnosis | Urinalysis, Blood test |
Differential diagnosis | N/A |
Prevention | N/A |
Treatment | Address underlying cause |
Medication | N/A |
Prognosis | N/A |
Frequency | N/A |
Deaths | N/A |
Phosphaturia is a medical condition characterized by the presence of an abnormally high concentration of phosphate in the urine. This condition can be indicative of various underlying disorders affecting phosphate metabolism and renal function.
Pathophysiology[edit | edit source]
Phosphaturia occurs when there is an imbalance in the renal handling of phosphate. Normally, the kidneys filter phosphate from the blood and reabsorb most of it back into the bloodstream. However, in phosphaturia, this reabsorption process is impaired, leading to increased excretion of phosphate in the urine.
The renal handling of phosphate is primarily regulated by the hormone parathyroid hormone (PTH), which increases phosphate excretion, and fibroblast growth factor 23 (FGF23), which also promotes phosphate excretion. Disruptions in the levels or activity of these hormones can lead to phosphaturia.
Causes[edit | edit source]
Phosphaturia can result from a variety of conditions, including:
- Renal tubular disorders: Conditions such as Fanconi syndrome can impair the renal tubules' ability to reabsorb phosphate.
- Hyperparathyroidism: Excessive secretion of PTH increases renal phosphate excretion.
- Vitamin D deficiency: Leads to decreased intestinal absorption of phosphate and increased renal excretion.
- Hereditary hypophosphatemic rickets with hypercalciuria: A genetic disorder affecting phosphate reabsorption.
Diagnosis[edit | edit source]
The diagnosis of phosphaturia involves:
- Urinalysis: To measure the concentration of phosphate in the urine.
- Blood test: To assess serum phosphate levels and evaluate for potential causes such as hyperparathyroidism or vitamin D deficiency.
- Renal function tests: To evaluate overall kidney function.
Treatment[edit | edit source]
Treatment of phosphaturia focuses on addressing the underlying cause. For example:
- In cases of hyperparathyroidism, surgical removal of the overactive parathyroid gland may be necessary.
- Vitamin D supplementation can be used to correct vitamin D deficiency.
- Management of renal tubular disorders may involve electrolyte replacement and supportive care.
Complications[edit | edit source]
If left untreated, phosphaturia can lead to complications such as:
- Hypophosphatemia: Low levels of phosphate in the blood, which can cause muscle weakness and bone pain.
- Osteomalacia: Softening of the bones due to phosphate depletion.
Also see[edit | edit source]
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Contributors: Prab R. Tumpati, MD