hyperphosphaturia


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hyperphosphaturia

 [hi″per-fos″fah-tu´re-ah]
an excessive amount of phosphates in the urine, such as in hyperparathyroidism, rickets, or inability of renal tubules to reabsorb phosphorus.

hy·per·phos·pha·tu·ri·a

(hī'pĕr-fos'fă-tyū'rē-ă),
An increased excretion of phosphates in the urine.

hyperphosphaturia

/hy·per·phos·pha·tu·ria/ (-fos″fah-tu´re-ah) an excess of phosphates in the urine.

hyperphosphaturia

(hī′pər-fŏs′fə-to͝or′ē-ə)
n.
An increased excretion of phosphates in the urine.

hy·per·phos·pha·tu·ri·a

(hī'pĕr-fos'fă-tyūr'ē-ă)
An increased excretion of phosphates in the urine.

hy·per·phos·pha·tu·ri·a

(hī'pĕr-fos'fă-tyūr'ē-ă)
An increased excretion of phosphates in the urine.

hyperphosphaturia (hī´purfos´fə-too´rēə),

n an excessive excretion of phosphate in the urine.

hyperphosphaturia

an excess of phosphates in the urine.
References in periodicals archive ?
Patients with tumor-induced osteomalacia are characterized biochemically by hypophosphatemia, hyperphosphaturia, inappropriately low or normal 1,25-dihydroxyvitamin D concentration, and increased alkaline phosphatase concentration.
described high urine carnitine concentration, aminoacyduria and hyperphosphaturia in CF patient with coexisting renal tubules defect [19].
Hypercalciuria, hyperphosphaturia, hypocitraturia and a high urinary pH are the main events that predispose RTA patients to develop renal stones.
One study reported that 22% of patients on tenofovir developed at least 2 out of 6 features of proximal tubular dysfunction such as hyperaminoaciduria, glycosuria in the presence of normoglycaemia, and hyperphosphaturia.
Hyperaminoaciduria and hyperphosphaturia occur as a result of 20HPT.
Severe hyperaminoaciduria and hyperphosphaturia occur in this stage as a result of severe 20HPT.
Oncogenic osteomalacia is an unusual syndrome that is characterized by multiple biochemical abnormalities, such as hypophosphatemia, hyperphosphaturia, and low levels of plasma 1,25-dihydroxyvitamin D.
Hypophosphatemic rickets (HR) is a rare genetic disorder, which is characterised by diminished phosphate reabsorption in renal tubules leading to chronic hyperphosphaturia and hypophosphatemia, which are associated with normal or low levels of 1,25(OH)2 Vitamin D3.
Laboratory Findings in these patients show hypophosphataemia with hyperphosphaturia, normocalcaemia with normal or reduced calciuria [Jan and Levine, 2008].
Those authors described a clinical case of rickets, with hypophosphataemia and hyperphosphaturia resistant to normal doses of vitamin D, and classified this metabolic condition as inheritable X-linked hypophosphataemic rickets (XLHR).