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Melorheostosis: Report of a new case with linear scleroderma

dc.contributor.authorEryavuz, M
dc.contributor.authorTuzun, F
dc.contributor.authorUnalan, H
dc.contributor.authorBirtane, M
dc.date.accessioned2021-03-04T10:31:41Z
dc.date.available2021-03-04T10:31:41Z
dc.date.issued1998
dc.identifier.citationBirtane M., Eryavuz M., Unalan H., Tuzun F., "Melorheostosis: Report of a new case with linear scleroderma", CLINICAL RHEUMATOLOGY, cilt.17, sa.6, ss.543-545, 1998
dc.identifier.issn0770-3198
dc.identifier.otherav_6da534c5-f266-4d45-ab10-34c206e10ae9
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/75729
dc.identifier.urihttps://doi.org/10.1007/bf01451298
dc.description.abstractMelorheostosis is a very rare bone disease of unknown etiology characterised by linear hyperostosis and associated with fibrosis of soft tissues and the skin. This uncommon sclerosing bone dysplasia was first described by Leri and Joanny in 1922, and since then, until 1993, approximately 300 cases were reported in the literature. Linear scleroderma is a localised proliferation of connective tissue and has rarely been associated with melorheostosis.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleMelorheostosis: Report of a new case with linear scleroderma
dc.typeMakale
dc.relation.journalCLINICAL RHEUMATOLOGY
dc.contributor.department, ,
dc.identifier.volume17
dc.identifier.issue6
dc.identifier.startpage543
dc.identifier.endpage545
dc.contributor.firstauthorID120163


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