Karabacakoğlu, AydınKaraköse, SerdarDeniz, ErgünÖdev, Kemal2020-03-262020-03-262001Karabacakoğlu, A., Karaköse, S., Deniz, E., Ödev, K., (2001). Hurler Sendromunda Kranial MRG Bulguları. Türkiye Klinikleri Tıp Bilimleri Dergisi, 21(6), 503-507.1300-02922146-9040http://www.trdizin.gov.tr/publication/paper/detail/TVRZMU1UQXc=https://hdl.handle.net/20.500.12395/17446Mukopolisakkaridozisin klinik olarak ağır formlarından biri olan Hurler sendromu, mukopolisakkaridozisin prototipi olup, a-L-iduronidaz eksikliği sonucu gelişir. Klinik ve radyolojik incelemeleri sonucunda Hurler sendromu tanısı alan bir olgunun diğer radyolojik bulguları ile birlikte kranial manyetik rezonans görüntüleme bulguları sunuldu.The Hurler's syndrome which was caused by lack of a-L-iduronidase is a prototypical mucopolysaccharidosis and this is one of the more severe forms. Cranial magnetic resonance imaging and characteristic conventional radiologic findings are reported in a patient with Hurler's syndrome. The diagnosis was confirmed clinically and radiologically.trinfo:eu-repo/semantics/openAccessHurlerMukopolisakkaridozisKranialMRGMucopolysaccharidosisCranialMRIOther216503507