Facial-muscle weakness, speech disorders and dysphagia are common in patients with classic infantile Pompe disease treated with enzyme therapy

Classic infantile Pompe disease is an inherited generalized glycogen storage disorder caused by deficiency of lysosomal acid α-glucosidase. If left untreated, patients die before one year of age. Although enzyme-replacement therapy (ERT) has significantly prolonged lifespan, it has also revealed new...

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Detalles Bibliográficos
Autores principales: van Gelder, C. M., van Capelle, C. I., Ebbink, B. J., Moor-van Nugteren, I., van den Hout, J. M. P., Hakkesteegt, M. M., van Doorn, P. A., de Coo, I. F. M., Reuser, A. J. J., de Gier, H. H. W., van der Ploeg, A. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319904/
https://www.ncbi.nlm.nih.gov/pubmed/22008944
http://dx.doi.org/10.1007/s10545-011-9404-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319904/
https://www.ncbi.nlm.nih.gov/pubmed/22008944
http://dx.doi.org/10.1007/s10545-011-9404-7

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