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- W4313458658 abstract "Hurler syndrome (HS) belongs to the category of mucopolysaccharidosis (MPS), a spectrum of rare genetic disorders of the mucopolysaccharides metabolism. This syndrome is due to a defect in α-iduronidase, an enzyme responsible for the degradation of the glycosaminoglycans (GAGs) heparin and dermatan sulfate. Intra and extracellular accumulation of these non-metabolized substances may lead to multisystemic dysfunction, with severe stomatognathic involvement that may often need treatment. The aim of this article is to present the heterogeneity of orofacial and radiographic findings observed in two patients with HS with long-term follow-up, who were referred to our Stomatology department." @default.
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- W4313458658 date "2023-01-03" @default.
- W4313458658 modified "2023-10-14" @default.
- W4313458658 title "Hurler Syndrome: Orofacial Clinical Findings" @default.
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- W4313458658 doi "https://doi.org/10.7759/cureus.33313" @default.
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