Importance of Timely Treatment Initiation in Infantile-Onset Pompe Disease, a Single-Centre Experience

Classic infantile Pompe disease (IPD) is a rare lysosomal storage disorder characterized by severe hypertrophic cardiomyopathy and profound muscle weakness. Without treatment, death occurs within the first 2 years of life. Although enzyme replacement therapy (ERT) with alglucosidase alfa has improve...

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Autores principales:	Javier de las Heras, Ainara Cano, Ana Vinuesa, Marta Montes, María Unceta Suarez, Arantza Arza, Saioa Jiménez, Elena Vera, Marta del Hoyo, Miriam Gendive, Lizar Aguirre, Gisela Muñoz, Javier Fernández, Cynthia Ruiz-Espinoza, María Ángeles Fernández, José Miguel Galdeano, Irene Rodríguez, Lourdes Román, Amaya Rodríguez-Serna, Begoña Loureiro, Itziar Astigarraga
Formato:	article
Lenguaje:	EN
Publicado:	MDPI AG 2021
Materias:	Pompe disease infantile Pompe disease immune tolerance induction immunomodulation early diagnosis enzyme replacement therapy Pediatrics RJ1-570
Acceso en línea:	https://doaj.org/article/05147c9eb1a64757918d5361ca6ff5e4
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Importance of Timely Treatment Initiation in Infantile-Onset Pompe Disease, a Single-Centre Experience

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