An idiopathic case of calcium pyrophosphate dihydrate crystal deposition disease with crowned dens syndrome in a young patient

dc.contributor.authorUnlu Z.
dc.contributor.authorTarhan S.
dc.contributor.authorOzmen E.M.
dc.date.accessioned2025-04-10T11:16:02Z
dc.date.available2025-04-10T11:16:02Z
dc.date.issued2009
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. Copyright © 2009 by The Southern Medical Association.
dc.identifier.DOI-ID10.1097/SMJ.0b013e3181b08c26
dc.identifier.urihttp://hdl.handle.net/20.500.14701/51496
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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