X-linked hypophosphatemia (XLH), also known as hereditary type I hypophosphatemia (HPDR I) or familial hypophosphatemia, is an inherited, chronic condition that causes your body to lose phosphate.

X-linked hypophosphatemia (XLH) is a rare genetic disease that causes your body to release phosphorus through your urine. The excessive wasting of phosphorus leads to low levels of phosphorus in the ...

Please provide your email address to receive an email when new articles are posted on . “Anemia is the most common extraintestinal manifestation of IBD, and iron deficiency and inflammation are its ...

Nat Clin Pract Nephrol. 2006;2(3):136-148. Another musculoskeletal condition associated with hypophosphatemia is hypophosphatemic osteomalacia. Patients with this condition generally have proximal ...

J Glaucoma. 2015;24(4):E31-e33. In our case, the patient presented with typical features of hypophosphatemia including general weakness, hypercapnic respiratory failure, arrhythmias, and cardiac ...

In a patient with chronic renal disease and uremia who was under treatment with a low-protein diet, hemodialysis and aluminum hydroxide gel marked hypophosphatemia associated with anorexia, nausea, ...

X-linked hypophosphatemia (XLH) is the most common cause of hereditary rickets in children. The early detection of XLH is crucial to appropriate pediatric management, surveillance for complications ...

Cost-effectiveness of denosumab (Dmab) versus zoledronic acid (ZA) for prevention of skeletal-related events (SREs) in patients (pts) with castrate-resistant prostate cancer (CRPC) and bone metastases ...

In X-linked hypophosphatemia, phosphate wasting results from increased circulating levels of fibroblast growth factor 23 (FGF-23). 1 Administration of calcitonin to a patient with oncogenic ...

X-linked hypophosphatemia (XLH) is the classical bone disorder caused by renal wasting of the phosphate. Formerly called vitamin D-resistant rickets, it is the most frequently observed condition among ...