Ameloblastoma in a Three-Year-Old Child with Hurler Syndrome (Mucopolysaccharidosis Type I)

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...

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Bibliographic Details
Main Authors: Mattia Di Bartolomeo, Arrigo Pellacani, Sara Negrello, Martina Buchignani, Riccardo Nocini, Gianluca Di Massa, Greta Gianotti, Giuseppe Pollastri, Giacomo Colletti, Luigi Chiarini, Alexandre Anesi
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Reports
Subjects:
Online Access:https://www.mdpi.com/2571-841X/5/1/10