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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Main Authors: Consuelo Cantú-Reyna (Author), Diana Laura Vazquez-Cantu (Author), Héctor Cruz-Camino (Author), Yuriria Arlette Narváez-Díaz (Author), Óscar Flores-Caloca (Author), Óscar González-Llano (Author), Carolina Araiza-Lozano (Author), René Gómez-Gutiérrez (Author)
Format: Book
Published: MDPI AG, 2023-03-01T00:00:00Z.
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