2022
DOI: 10.3390/reports5010010
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Ameloblastoma in a Three-Year-Old Child with Hurler Syndrome (Mucopolysaccharidosis Type I)

Abstract: Mucopolysaccharidoses (MPS) are a family of genetic diseases associated with a deficiency of alpha-L iduronidase, which causes a lack of catabolism of glycosaminoglycans (GAGs). Therefore, the accumulation of GAGs determines a wide spectrum of symptoms, typically found in a few syndromes like Hurler syndrome (HS). Among other specific manifestations, craniofacial abnormalities are crucial for the characterization of this syndrome. Ameloblastoma is a rare, benign, slow-growing, odontogenic tumor usually located… Show more

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“…The differential diagnosis for patients presenting with lytic lesions is broad and depends on the patient's age and the presence of other systemic disease [22][23][24].…”
Section: Discussionmentioning
confidence: 99%
“…The differential diagnosis for patients presenting with lytic lesions is broad and depends on the patient's age and the presence of other systemic disease [22][23][24].…”
Section: Discussionmentioning
confidence: 99%