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 .
9 g/day, and hyperphosphaturia
was defined as a urinary phosphorus level more than 1.
, 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).