The Outcome of Infantile Onset Pompe Disease in South of Iran

BACKGROUND: Infantile Onset Pompe Disease (IOPD) is a rare autosomal recessive neuromuscular disorder. It is associated with cardiomegaly, hypotonia, paresis, and death in the first year of life. Since 2006, following the use of Alglucosidase alfa as Enzyme Replacement Therapy (ERT), the patients’ s...

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Detalles Bibliográficos
Autores principales: Moravej, Hossein, Karamizadeh, Zohre, Paran, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4733296/
https://www.ncbi.nlm.nih.gov/pubmed/26848380
http://dx.doi.org/10.5812/ijp.4473

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