Publication:
Dyggve-Melchior-Clausen Syndrome without Mental Retardation (Smith-McCort Dysplasia)

dc.contributor.authorBayrak I.K.
dc.contributor.authorNural M.S.
dc.contributor.authorDiren H.B.
dc.date.accessioned2020-06-21T09:23:32Z
dc.date.available2020-06-21T09:23:32Z
dc.date.issued2005
dc.departmentOMÜen_US
dc.department-tempBayrak, I.K., Department of Radiology, Ondokuz Mayis University School of Medicine, Samsun, Turkey -- Nural, M.S., Department of Radiology, Ondokuz Mayis University School of Medicine, Samsun, Turkey -- Diren, H.B., Department of Radiology, Ondokuz Mayis University School of Medicine, Samsun, Turkey --en_US
dc.description.abstractRadiographic features of a 15-year-old boy with Smith-McCort dysplasia are presented. Dyggve-Melchior-Clausen syndrome without mental retardation has clinical and radiographic findings similar to those of Smith-McCort dysplasia. Both of these syndromes are rare autosomal recessive disorders affecting skeletal development. The radiographic appearance of generalized platyspondyly with double-humped end-plates, and the lace-like appearance of iliac crests are pathognomonic and distinctive of these syndromes. Diagnostic features of these diseases are compared with others like Morquio's disease and spondylometaphyseal dysplasia, which may have similar vertebral changes, and are discussed in the light of the literature. © Turkish Society of Radiology 2005.en_US
dc.identifier.endpage165en_US
dc.identifier.issn1305-3825
dc.identifier.issue3en_US
dc.identifier.pmid16206059
dc.identifier.startpage163en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3587
dc.identifier.volume11en_US
dc.language.isoenen_US
dc.relation.journalDiagnostic and Interventional Radiologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBone Disease, Developmentalen_US
dc.subjectMental Retardationen_US
dc.titleDyggve-Melchior-Clausen Syndrome without Mental Retardation (Smith-McCort Dysplasia)en_US
dc.typeArticleen_US
dspace.entity.typePublication

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