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dc.contributor.authorTunaci, M.
dc.contributor.authorCefle, K.
dc.contributor.authorPalanduz, S.
dc.contributor.authorOzturk, S.
dc.contributor.authorCefle, A.
dc.date.accessioned2021-03-04T12:12:56Z
dc.date.available2021-03-04T12:12:56Z
dc.date.issued2006
dc.identifier.citationCefle A., Cefle K., Tunaci M., Ozturk S., Palanduz S., "A case of progressive pseudorheumatoid arthropathy of 'childhood' with the diagnosis delayed to the fifth decade", INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, cilt.60, sa.10, ss.1306-1309, 2006
dc.identifier.issn1368-5031
dc.identifier.otherav_762c33a5-4682-41d9-943a-9359df937cc5
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/81161
dc.identifier.urihttps://doi.org/10.1111/j.1742-1241.2005.00662.x
dc.description.abstractProgressive pseudorheumatoid arthropathy of childhood (PPAC) is a rare single gene disorder which is frequently misdiagnosed as juvenile rheumatoid arthritis. It is characterised with arthralgia, joint contractures, bony swelling of metacarpophalangeal and interphalangeal joints and platyspondyly. Clinical and laboratory signs of joint inflammation such as synovitis, a high erythrocyte sedimentation rate and an elevated C-reactive protein level are usually absent. Although the disease begins early in life (usually between 3 and 8 years of age), the diagnosis may be delayed. In the present case report, we describe a male patient diagnosed with PPAC at the age of 46 years, although he had been exhibiting the typical radiological and clinical features of the disease since the age of 7 years.
dc.language.isoeng
dc.subjectTemel Tıp Bilimleri
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleA case of progressive pseudorheumatoid arthropathy of 'childhood' with the diagnosis delayed to the fifth decade
dc.typeMakale
dc.relation.journalINTERNATIONAL JOURNAL OF CLINICAL PRACTICE
dc.contributor.department, ,
dc.identifier.volume60
dc.identifier.issue10
dc.identifier.startpage1306
dc.identifier.endpage1309
dc.contributor.firstauthorID13020


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