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HURLER SENDROMU’NUN (MUKOPOLİSAKKARİDOZ-I) ORAL BULGULARI: OLGU SUNUMU
Author(s) -
Zeki Arslanoğlu,
Ahmet Altan,
Halenur Onat,
Soydan Kılıç,
İbrahim Damlar
Publication year - 2015
Publication title -
dergipark (istanbul university)
Language(s) - English
DOI - 10.17944/mkutfd.70858
Subject(s) - medicine
Hurler syndrome (Mucopolysaccharidosis type I) is one of the genetic disorders involving disturbances in mucopolysaccharide metabolism resulting in increased storage of acid mucopolysaccharide in various tissues. An 7-year-old girl with Hurler syndrome is described in this article, with special emphasis on the oral, dental and radiographic findings. Key Mucopolysaccharidosis type I, oral finding, dentistywords: Hurler syndrome

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