Introduction: X-Linked Hypophosphatemic Rickets (XLHR) occurs due to mutations in PHEX gene leading to a disordered production of FGF23 and hypophosphatemia. This disease is characterized by bowing of lower extremities. Phosphate...
moreIntroduction: X-Linked Hypophosphatemic Rickets (XLHR) occurs due to mutations in PHEX gene leading to a disordered production of FGF23 and hypophosphatemia. This disease is characterized by bowing of lower extremities. Phosphate supplements and oral vitamin medications, partially or, in some cases, fully restore the straightness of the limbs. Surgery is considered a vital alternative for severe or residual limb deformities in adolescent population. Case Report: A 19 year old male presented to us with complaints of bilateral bowing of lower extremities, diagnosed to be X-Linked Hypophosphatemic Rickets .He underwent correction of deformity in both femurs, spaced 5 months apart, with intramedullary nailing, based on the principle of CORA. Follow-up period of 3 years showed a good functional outcome from the patient with no complications acquired so far. Patient gained a height of 5 cms. Discussion: The treatment for XLHR, principally, starts with rectifying hypophosphatemia and, is Case Study