Publication:
Yenidoğanda Rizomelik Kondrodisplazi Punktata ve Foramen Magnum Stenozu

dc.contributor.authorYalın, C. Türkay
dc.contributor.authorBayrak, İlkay Koray
dc.contributor.authorDanacı, Murat
dc.contributor.authorİncesu, Lütfi
dc.date.accessioned2020-06-21T10:31:13Z
dc.date.available2020-06-21T10:31:13Z
dc.date.issued2003
dc.departmentOMÜen_US
dc.department-tempOndokuz Mayıs Üniversitesi, Tıp Fakültesi, Radyoloji Anabilim Dalı, Samsun, Türkiye -- Girilmedi -- Girilmedi -- Girilmedi -- ONDOKUZ MAYIS ÜNİVERSİTESİ -- Tanımlanmamış Kurum -- Tanımlanmamış Kurumen_US
dc.description.abstractChondrodysplasia punctata is a peroxisomal disorder which is a form of multiple epiphyseal dysplasia. It is characterized by calcifications of unossified cartilaginous epiphyseal centers during the first year of life. Severe autosomal recessive rhisomelic form shows bilateral proximal shortening of the upper and lower limbs with punctate epiphyseal calcifications. We report radiological findings of a patient with rhisomelic chondrodysplasia punctata. Magnetic resonance imaging showed foramen magnum stenosis that caused spinal cord compression.en_US
dc.identifier.endpage103en_US
dc.identifier.issn1300-4360
dc.identifier.issue1en_US
dc.identifier.startpage100en_US
dc.identifier.urihttps://app.trdizin.gov.tr/publication/paper/detail/TWpJeE5UQXc=
dc.identifier.urihttps://hdl.handle.net/20.500.12712/8234
dc.identifier.volume9en_US
dc.language.isotren_US
dc.relation.journalTanısal ve Girişimsel Radyoloji (Yeni Adı: Dİagnostic & Intervent. Radiol)en_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectRadyolojien_US
dc.subjectNükleer Tıpen_US
dc.subjectTıbbi Görüntülemeen_US
dc.titleYenidoğanda Rizomelik Kondrodisplazi Punktata ve Foramen Magnum Stenozuen_US
dc.title.alternativeCase report: Rhisomelic chondrodypslasia punctata and foramen magnum stenosis in a newbornen_US
dc.typeArticleen_US
dspace.entity.typePublication

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