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This research article explores FGF-23 driven hypophosphatemia caused by phosphaturic tumors, highlighting its diagnostic challenges and the importance of advanced imaging techniques. The study presents a case of a young male with severe hypophosphatemia and osteomalacia due to a phosphaturic mesenchymal tumor, which was successfully diagnosed and treated through surgical resection. The findings emphasize the need for clinical awareness and a multidisciplinary approach in managing such rare conditions.

Author

pirzahoor

Language

EN