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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Detalles Bibliográficos
Autores principales: Cantú-Reyna, Consuelo, Vazquez-Cantu, Diana Laura, Cruz-Camino, Héctor, Narváez-Díaz, Yuriria Arlette, Flores-Caloca, Óscar, González-Llano, Óscar, Araiza-Lozano, Carolina, Gómez-Gutiérrez, René
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136708/
https://www.ncbi.nlm.nih.gov/pubmed/37189891
http://dx.doi.org/10.3390/children10040642

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136708/
https://www.ncbi.nlm.nih.gov/pubmed/37189891
http://dx.doi.org/10.3390/children10040642

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