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CASE REPORT
A case of craniofacial fibrous dysplasia associated with McCune-Albright syndrome lost to follow-up
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  1. Robert Gareth Michael Williams
  1. Department of Oral and Maxillofacial, Aintree University Hospital, Liverpool, UK
  1. Correspondence to Dr Robert Gareth Michael Williams, robwilliams{at}hotmail.co.uk

Summary

McCune-Albright syndrome is a rare fibro-osseous syndrome characterised by a classic triad of fibrous dysplasia (FD), café-au-lait macules and various underlying endocrinopathies. This case report describes how a patient was rediagnosed by a general dental practitioner following attendance for a routine dental examination. The patient had been previously diagnosed with the condition 28 years earlier but no follow-up or monitoring of her condition had taken place. As a result, she was found to have several undiagnosed and untreated complications of the disease including FD of the mandible, optic neuropathy and potential thyroid involvement.

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