Hurler Sendromunda Kranial MRG Bulguları
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Dosyalar
Tarih
2001
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Mukopolisakkaridozisin 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.
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.
Açıklama
Anahtar Kelimeler
Hurler, Mukopolisakkaridozis, Kranial, MRG, Mucopolysaccharidosis, Cranial, MRI
Kaynak
Türkiye Klinikleri Tıp Bilimleri Dergisi
WoS Q Değeri
Scopus Q Değeri
Cilt
21
Sayı
6
Künye
Karabacakoğlu, A., Karaköse, S., Deniz, E., Ödev, K., (2001). Hurler Sendromunda Kranial MRG Bulguları. Türkiye Klinikleri Tıp Bilimleri Dergisi, 21(6), 503-507.
