Contemporary Medical and Surgical Management of X-linked Hypophosphatemic Rickets.

Melinda S Sharkey, Karl Grunseich, Thomas O Carpenter

Journal: The Journal of the American Academy of Orthopaedic Surgeons 2015;23(7):433-42

PMID: 26040953

Abstract

X-linked hypophosphatemia is an inheritable disorder of renal phosphate wasting that clinically manifests with rachitic bone pathology. X-linked hypophosphatemia is frequently misdiagnosed and mismanaged. Optimized medical therapy is the cornerstone of treatment. Even with ideal medical management, progressive bony deformity may develop in some children and adults. Medical treatment is paramount to the success of orthopaedic surgical procedures in both children and adults with X-linked hypophosphatemia. Successful correction of complex, multiapical bone deformities found in patients with X-linked hypophosphatemia is possible with careful surgical planning and exacting surgical technique. Multiple methods of deformity correction are used, including acute and gradual correction. Treatment of some pediatric bony deformity with guided growth techniques may be possible.

Copyright 2015 by the American Academy of Orthopaedic Surgeons.

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