Morquio's syndrome: Clinical and radiological aspects

dc.contributor.authorAydin, Mustafa
dc.contributor.authorArtaş, Hakan
dc.contributor.authorErtu?rul, Sabahattin
dc.contributor.authorYilmaz, Hüseyin
dc.date.accessioned2026-08-12T16:15:46Z
dc.date.issued2006
dc.departmentFırat Üniversitesi
dc.description.abstractMorquio's syndrome is an inherited disorder caused by the lack of the enzyme responsible for breakdown of keratan sulfate. The resulting buildup of keratan sulfate in tissues leads to skeletal dysplasia with other organ systems involvement. A four years old girl brought with the complaints of deformity in legs, abnormal gait, changed shape of chest cage, and short trunk dwarfism was presented to emphasize the clinical and radiological features of the Morquio's syndrome. Morquio's syndrome should be also considered in the differential diagnosis of the patients with short trunk dwarfism and skeletal deformities.
dc.identifier.endpage152
dc.identifier.issn1300-526X
dc.identifier.issue3
dc.identifier.scopus2-s2.0-33845660273
dc.identifier.scopusqualityN/A
dc.identifier.startpage149
dc.identifier.urihttps://hdl.handle.net/11508/43878
dc.identifier.volume21
dc.indekslendigikaynakScopus
dc.language.isotr
dc.relation.ispartofGoztepe Tip Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20260511
dc.subjectKeratan sulfate; Morquio's syndrome; Radiological finding; Short trunk dwarfism
dc.titleMorquio's syndrome: Clinical and radiological aspects
dc.title.alternativeMorquio sendromu: Klinik ve radyolojik yönden de?erlendirme
dc.typeArticle

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