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Creutzfeldt-Jakob disease affecting the maxillofacial region: a case report
Khalid Abdel-Galil1, Christy Williams, Paul Chambers
1Bradford Teaching Hospitals NHS Foundation Trust, St. Luke's Hospital, Bradford, United Kingdom. khalidabdelgalil@doctors.org.uk
Abstract:
Creutzfeldt-Jakob disease (CJD) is a rare disorder caused by prions that can affect any part of the central nervous system. It is characterised by an initial non-specific illness of varying duration, followed by progressive neurological decline. We report a patient with sporadic CJD who presented with neurological symptoms and bilateral dislocation of the temporomandibular joints (TMJs). To our knowledge this is the first report of sporadic CJD that involved the maxillofacial region.
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