Mucopolysaccharidosis Type I in Mexico: Case-Based Review

Mucopolysaccharidosis Type I in Mexico: Case-Based Review

Introduction: Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disease present in 1:100,000 newborns. Variants in the IDUA (alpha-L-iduronidase) gene decrease the enzyme activity for glycosaminoglycans metabolism. MPS I patients exhibit clinical manifestations that fall on the Hurler, Hur...

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Bibliographic Details
Main Authors: Consuelo Cantú-Reyna, Diana Laura Vazquez-Cantu, Héctor Cruz-Camino, Yuriria Arlette Narváez-Díaz, Óscar Flores-Caloca, Óscar González-Llano, Carolina Araiza-Lozano, René Gómez-Gutiérrez
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Children
Subjects:
Mucopolysaccharidosis I
Mexico
iduronidase
Online Access:https://www.mdpi.com/2227-9067/10/4/642

Internet

https://www.mdpi.com/2227-9067/10/4/642

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