An Idiopathic Case of Calcium Pyrophosphate Dihydrate Crystal Deposition Disease with Crowned Dens Syndrome in a Young Patient

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dc.contributor.authorUnlu, Z
dc.contributor.authorTarhan, S
dc.contributor.authorOzmen, EM
dc.date.accessioned2024-07-18T11:49:13Z
dc.date.available2024-07-18T11:49:13Z
dc.description.abstractCalcium pyrophosphate dihydrate (CPPD) crystal deposition disease is rare in patients under the age of 40 in the absence of metabolic or familial predisposition. A high incidence of involvement of the transverse ligament of the atlas in CPPD deposition disease was reported. However, involvement of the craniocervical junction is rarely symptomatic. We report a rare case in a young male with severe idiopathic CPPD crystal deposition disease, including crowned dens syndrome in the cervical spine.
dc.identifier.issn0038-4348
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/3868
dc.language.isoEnglish
dc.publisherLIPPINCOTT WILLIAMS & WILKINS
dc.subjectCPPD
dc.titleAn Idiopathic Case of Calcium Pyrophosphate Dihydrate Crystal Deposition Disease with Crowned Dens Syndrome in a Young Patient
dc.typeArticle

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