赫勒综合征：一罕见临床病例的口腔及影像学表现

Medical Reports Pub Date : 2025-07-28 DOI:10.1016/j.hmedic.2025.100325

W. Kabbassi, H. Hessissen, J. Hammouti

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引用次数: 0

摘要

Hurler综合征（HS）是一种罕见的粘多糖病（MPS），是由遗传性溶酶体α- l -伊杜糖醛酸酶活性不足引起的。HS患者具有特定的面部特征和几种口腔表现。我们通过这篇文章介绍了一个15岁的女孩，她被转介到拉巴特牙科咨询和治疗中心的儿科牙科部门，被诊断为有许多口腔表现的赫勒综合征。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Hurler syndrome: Oral and radiographic findings of a rare clinical case

Hurler syndrome (HS) is a rare disorder which belongs to the category of mucopolysaccharidosis (MPS) caused due to inherited deficiencies of lysosomal α-L-iduronidase activity. Individuals with HS share specific facial features with several oral manifestations. We present through this article a case of a 15-year-old girl that was referred to the pediatric dentistry department at the center of dental consultation and treatment of Rabat, diagnosed with Hurler- syndrome with numerous oral manifestations.

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Medical Reports

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