An adolescent girl complaining of chronic heel pain was found to have acquired hypophosphatemic rickets and a nonossifying fibroma of the femur. The hypophosphatemic rickets was completely corrected by surgical excision of the bone lesion. This case represents another example of tumor-induced osteomalacia. ACQUIRED primary hypophosphatemic~~&dquo;&dquo;3~II~~T ~ nma rickets is an uncommon disorder. In 1959 Prader et al.1 described such a patient who was found to have an osseous tumor. Upon excision of the tumor, the serum phosphorus concentration returned to normal and the rickets healed, In a review of the literature, we were able to find 16 additional cases of tumor-induced or tumor-related osteomalacia and rickets that have been ...
Osteomalacia in neurofibromatosis is a rare entity and distinct from more common dysplastic skeletal...
Tumor-induced osteomalacia (TIO), also known as oncogenic osteomalacia, is a rare acquired paraneopl...
We are going to present a case of hypo-phosphatemic rickets secondary to phosphaturic mesenchymal tu...
Osteomalacia is a condition characterised by failure of bonemineralisation. While abnormalities of v...
Tumor-induced osteomalacia (TIO) is a rare but potentially curable disease. It is caused by excessiv...
Tumor-induced hypophosphatemic osteomalacia is a rare disease and its diagnosis presents certain dif...
after resection of a deeply located soft-tissue tumour A.R.M. Radaideh md, * D. Jaradat md,* M.M. Ab...
Background:Tumor-induced osteomalacia (TIO), which is also known as oncogenic osteomalacia, is an un...
BACKGROUND: Tumor-induced hypophosphatemic osteomalacia is a syndrome characterized by urinary phosp...
Hypophosphatemic osteomalacia secondary to neopla-sia is an unusual clinical syndrome. Although rare...
Tumor-induced osteomalacia (TIO), also known as oncogenic osteomalacia, is a rare paraneoplastic syn...
Background Tumor-induced osteomalacia is a rare, acquired paraneoplastic syndrome, ...
Hypophosphatemic rickets is a disorder of bone mineralization caused due to defects (inherited/acqui...
Background: Tumor-associated fibroblast growth factor 23 (FGF-23)-induced hypophosphatemic rickets i...
Background: Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome characterized by rena...
Osteomalacia in neurofibromatosis is a rare entity and distinct from more common dysplastic skeletal...
Tumor-induced osteomalacia (TIO), also known as oncogenic osteomalacia, is a rare acquired paraneopl...
We are going to present a case of hypo-phosphatemic rickets secondary to phosphaturic mesenchymal tu...
Osteomalacia is a condition characterised by failure of bonemineralisation. While abnormalities of v...
Tumor-induced osteomalacia (TIO) is a rare but potentially curable disease. It is caused by excessiv...
Tumor-induced hypophosphatemic osteomalacia is a rare disease and its diagnosis presents certain dif...
after resection of a deeply located soft-tissue tumour A.R.M. Radaideh md, * D. Jaradat md,* M.M. Ab...
Background:Tumor-induced osteomalacia (TIO), which is also known as oncogenic osteomalacia, is an un...
BACKGROUND: Tumor-induced hypophosphatemic osteomalacia is a syndrome characterized by urinary phosp...
Hypophosphatemic osteomalacia secondary to neopla-sia is an unusual clinical syndrome. Although rare...
Tumor-induced osteomalacia (TIO), also known as oncogenic osteomalacia, is a rare paraneoplastic syn...
Background Tumor-induced osteomalacia is a rare, acquired paraneoplastic syndrome, ...
Hypophosphatemic rickets is a disorder of bone mineralization caused due to defects (inherited/acqui...
Background: Tumor-associated fibroblast growth factor 23 (FGF-23)-induced hypophosphatemic rickets i...
Background: Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome characterized by rena...
Osteomalacia in neurofibromatosis is a rare entity and distinct from more common dysplastic skeletal...
Tumor-induced osteomalacia (TIO), also known as oncogenic osteomalacia, is a rare acquired paraneopl...
We are going to present a case of hypo-phosphatemic rickets secondary to phosphaturic mesenchymal tu...