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Transition of patients with mucopolysaccharidosis from paediatric to adult care

Mucopolysaccharidoses (MPS) are rare disorders associated with enzyme deficiencies, resulting in glycosaminoglycan (GAG) accumulation in multiple organ systems. As patients increasingly survive to adulthood, the need for a smooth transition into adult care is essential. Using case studies, we outlin...

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Detalles Bibliográficos
Autores principales: Lampe, C., McNelly, B., Gevorkian, A.K., Hendriksz, C.J., Lobzhanidze, T.V., Pérez-López, J., Stepien, K.M., Vashakmadze, N.D., Del Toro, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819742/
https://www.ncbi.nlm.nih.gov/pubmed/31687335
http://dx.doi.org/10.1016/j.ymgmr.2019.100508