Glass, Lora R. DagiDagi, Teodoro ForchtDagi, Linda2013-02-152011Glass, Lora R. Dagi, Teodoro Forcht Dagi, and Linda R. Dagi. 2011. Papilledema in the setting of X-linked hypophosphatemic rickets with craniosynostosis. Case Reports in Ophthalmology 2(3): 376-381.1663-2699http://nrs.harvard.edu/urn-3:HUL.InstRepos:10304389Purpose: Introduction to the ophthalmic literature of an unusual cause of papilledema and subsequent optic atrophy: X-linked hypophosphatemic rickets (XLH). Methods: Case report of a 3-year-old female presenting with papilledema resulting from craniosynostosis secondary to XLH. Results: Early intervention with craniofacial surgery prevented the development of optic atrophy. Conclusion: Children with XLH should be screened for ophthalmic evidence of elevated intracranial pressure to aid early intervention and prevention of permanent loss of vision.en-USpapilledemaoptic atrophyricketscraniosynostosisJournal Article2013-02-1510.1159/000334941